Lediga jobb Dentsply Ih AB i Mölndal

Vill du vara med och driftsäkra vår produktion i Mölndal
Om rollen
I rollen som Maintenance Technician kommer du att arbeta med underhåll inom vår produktionsanläggning som innefattar bla bearbetnings- och förpackningsmaskiner.
Dina huvudsakliga arbetsuppgifter är;
Förebyggande och avhjälpande underhåll
Förbättringsarbete på våra maskinanläggningar
Driftsättning, förbättring och testning av nya maskiner och processer tillsammans med andra avdelningar
Driftsäkring av vår produktionsanläggning

Vem är du
Vi ser att du är drivande som person och du tycker om att medverka i förbättringsarbete i en produktionsmiljö med bla CNC maskiner, ytbehandling & förpackningsmaskiner. Du har en stor lust att lära dig nya saker och utvecklas i din roll.
Vi ser att du har
En gedigen dokumenterad teknisk kompetens inom drift och underhåll
Ett utmärkande kvalitetstänk och ett högt säkerhetstänk
En kostnadsmedvetenhet med fokus på effektivt och långsiktigt underhåll
En hög kommunikativ förmåga eftersom rollen innebär att du ska kunna kommunicera förtroendefullt, pedagogiskt och tydligt med personer på flera olika nivåer som har olika teknisk kunskap
Grundläggande PLC kunskaper


För mer information, ring gärna rekryterande chef, Jani Urpilainen på telefonnummer +46703192984
Ansökningar kommer att hanteras löpande, så skicka gärna in din ansökan snarast möjligt.
Om Dentsply Sirona
Dentsply Sirona är världens största tillverkare av tandvårdsprodukter och -lösningar, och har under 130 år erbjudit innovationer och service till tandvårdssektorn och patienter över hela världen. Dentsply Sirona utvecklar, tillverkar och marknadsför ett heltäckande utbud av produkter och lösningar för dental hälsa, liksom andra medicintekniska förbrukningsartiklar och har en stark varumärkesportfölj i världsklass. Dentsply Sirona marknadsför innovativa, högkvalitativa och effektiva lösningar för avancerad patientvård som ger bättre och säkrare tandvård. Dentsply Sironas globala huvudkontor ligger i Charlotte, North Carolina, USA. Företagets aktier är listade på amerikanska NASDAQ under symbolen XRAY. Visa mindre

We are looking for a BI Developer to join our Global Data, Business Intelligence and Analytics department in Molndal. The role is part of the team that is responsible for the development and implementation of global data and BI tools.
Why us you may ask?
You will be part of a global and cross functional setting where you will never stop learning. As our tech expert you will be working with the latest technology and platforms together with our data architects, data engineers and project managers to define and deliver the best solutions. In this role you work close to the business and will be expected to keep abreast of advancements in the BI Tools landscape. We have a high pace in everything that we do, and we take pride in our deliveries. We also love having fun at work and on Wednesdays we set the table for a Swedish fika. Team spirit is important for us!


Does this sound like the perfect challenge for you, then come join us!

This role provides 2nd Line support for BI Solutions, BI Platforms and Data Loading when required. We work in scrum team dedicated for finance and our corporate business function to be able to work close to them and support their business processes.
Responsibilities
What Will You Do?
Development of BI Solutions delivered through Power BI.
Education and training of internal users on BI Solutions.
Technical user support and updating user documentation.
Participant in the data modelling process for BI deliverables.
Participant in the delivery of a new BI self-service strategy and roll out to the different global functions.
Leading part in design and development of new BI solutions primarily using Power BI.
Evaluation and improvement of existing BI solutions and applications.
Technical Implementation of BI Solution within assigned projects.
Sizing of Work Items within assigned projects.
Additional responsibilities as assigned.


Background & Qualifications
Minimum 5 years of relevant work experience.
Extensive experience working in a BI environment preferably using Microsoft BI components.
English language – proficiency in verbal and written communication.


Who you are?
You have a pro-active mindset and an ease to build collaborative relationships with team members and stakeholders. Strong communication skills will be key as you will need to communicate clearly with both technical and non-technical users. To succeed in the role, you will need strong analytical skills as well strong presentation skills.
We will review applications continuously so please send in your application as soon as possible.
We look forward hearing from you! Visa mindre

Join our Quality Control team where we bring out the best in people in our effort to make a difference.
Responsibilities
As a Quality Technician you will perform final inspection and final release of products and make sure that all activities have been performed according to instructions.
The Quality Technician will perform several different activities within the group including:
Perform Incoming Inspection of components
Perform calibration of gauges
Perform measuring assignments
Be part of continuous improvement projects

Background/Qualifications
We think you are a positive and driven team player. You are open for challenges and enjoy working together with highly skilled and committed colleagues where every day makes a difference. We believe you have:
Minimum requirements:
High School/College or equivalent background
Analytic and structured approach
A careful, responsible way of working
Good writing skills as we have high demands on documentation.
Good communication and interpersonal skills as parts of the work is done in cross functional teams
Good knowledge of standard Microsoft Office applications
Language skills in Swedish. English skills are beneficial

Preferred requirements:
Experience of measurement instruments, such as calipers, micrometers etc.
Experience of measuring machines
Interest in machine programming
Thorough and detail oriented
Like repetitive work
Experience from regulated business
It is also considered an advantage if you are familiar with ISO 13485:2016 Medical Device – Quality Management System and FDA Quality System Regulation 21 CFR Part 820 or have experience from medical device or other product areas with high regulatory demands.

We look forward hearing from you, welcome with your application no later than March 17. Please note that we will review applications continuously, so be sure to send in your application as soon as possible.
About Dentsply Sirona
Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona’s products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona’s global headquarters is located in Charlotte, North Carolina, USA. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. Visa mindre

Ansvarsområde
Som Kvalitetstekniker kommer du att utföra slutkontroll och frisläpp av inkommande produkter samt se till att alla aktiviteter har utförts enligt gällande instruktioner.
Som kvalitetstekniker kommer du att:
utföra inkommande inspektion av komponenter
kalibrera tolkar
utföra mätuppdrag
ingå i projekt för ständiga förbättringar

Bakgrund/Kvalifikationer
Vi ser att du är en positiv och driven lagspelare. Du är öppen för utmaningar och tycker om att arbeta tillsammans med mycket duktiga och engagerade kollegor där varje dag gör skillnad. Vi tror att du:
Minimikrav:
har gymnasieutbildning, YH-utbildning eller liknande bakgrund
är analytisk och strukturerad
är noggrann och ansvarsfull
kan uttrycka dig väl i skrift då vi har höga krav på dokumentation
samarbetar och kommunicerar väl med andra då delar av arbetet sker i tvärfunktionella team
har goda kunskaper i Microsoft Office-paketet
talar och förstår svenska, kunskaper i engelska är önskvärt

Önskade krav:
erfarenhet av mätinstrument, såsom skjutmått, mikrometrar, mm
erfarenhet av mätmaskiner
intresse för maskinprogrammering
noggrann och detaljorienterad
gillar repetitivt arbete
erfarenhet från reglerad verksamhet

Det är meriterande om du är bekant med ISO 13485:2016 Medical Device – Quality Management System och FDA Quality System Regulation 21 CFR Part 820.Vi ser gärna att du har erfarenhet från medicintekniska produkter eller andra produktområden med höga regulatoriska krav.
Välkommen med din ansökan, vi kommer att granska ansökningar löpande, så se till att skicka in din ansökan så snart som möjligt.
Om Dentsply Sirona
Dentsply Sirona är världens största tillverkare av tandvårdsprodukter och -lösningar, och har under 130 år erbjudit innovationer och service till tandvårdssektorn och patienter över hela världen. Dentsply Sirona utvecklar, tillverkar och marknadsför ett heltäckande utbud av produkter och lösningar för dental hälsa, liksom andra medicintekniska förbrukningsartiklar och har en stark varumärkesportfölj i världsklass. Dentsply Sirona marknadsför innovativa, högkvalitativa och effektiva lösningar för avancerad patientvård som ger bättre och säkrare tandvård. Dentsply Sironas globala huvudkontor ligger i Charlotte, North Carolina, USA. Företagets aktier är listade på amerikanska NASDAQ under symbolen XRAY. Visa mindre

Join our QA Team! We bring out the best in people with our effort to make people smile. We are currently looking for several Quality Engineers in our Quality Assurance organizations, Dentsply Sirona. The Quality Engineers will be based in Mölndal Sweden.
The main objective for the position is to secure Quality Assurance for Products and Processes within DentsplySirona Implants. The Quality Engineer (QE) will work close with Manufacturing and either lead or take part in Improvement Projects.
As a QE you will work in a Global Environment and be part of a cross functional teams. Implementation of new way of working requires close cooperation with other functions either local or global. Close cooperation with other Manufacturing sites within the Dentsply Sirona organization.
Responsibilities:
Perform Process and System Improvements.
Facilitate root cause investigations for CAPA and NC Process.
When needed, lead and coordinate market actions when occur.
Perform QA review of Process Validation activities.
Actively be part in Design Transfer activities with QA knowledge.
Participate as QA representative in New Development Project.
Act as Internal Auditor according to audit plan.
External Audits, be part of preparation, execution and follow up.
Document Control, provide knowledge and support to the organisation.
Manage Calibration Process and secure compliance.
Support Manufacturing team with QA knowledge and guidance.
Perform Measurement System Analysis (MSA).


Who you are
For this role in a truly global business environment, we look for qualified candidates with a relevant background:
An academic degree in engineering or equivalent professional background
experience from working in the medical device industry and have knowledge about
ISO 13485, 21 CFR Part 820 and EU Medical Device Regulation 2017/745
experience from Product and Process Validations
trained in Six Sigma, Gauge R&R and MiniTab
knowledge in measurement techniques for medical device
excellent communication skills as the role requires close contact with several functions/sites
participation in and experience of Audits from external parties
good communication in English as well as Swedish, both written and verbally.


If you have worked as a Lead Auditor and/or have good knowledge in the statistical area this is an advantage.
We look for a colleague with analytical skills, attention to details and the ability to work both in cross functional team and independently. We believe that you are a positive and social person with the ability to maintain good relations with both external and internal contacts. It is an advantage if you have strong focus on and drive to achieve goals and targets. As you will be working in a global environment, your English must be excellent, written and spoken alike.


We look forward hearing from you, welcome with your application no later than October 8th. Please note that we will review applications continuously, so be sure to send in your application as soon as possible. Visa mindre

Join our Quality Control team where we bring out the best in people in our effort to make a difference.
Responsibilities
As a Quality Technician you will perform incoming inspection, final inspection and final release of products and make sure that all activities have been performed according to instructions.
The Quality Technician will perform several different activities within the group including:
Inspection of sterile and non-sterile product documentation.
Perform Incoming Inspection of components.
Be part of continuous improvement projects.
Archiving of batch documentation.


Background/Qualifications
We think you are a positive and driven team player. You are open for challenges and enjoy working together with highly skilled and committed colleagues where every day makes a difference. We believe you have:
Minimum requirements:
High School/College or equivalent background
Analytic and structured approach
A careful, responsible way of working.
Good writing skills as we have high demands on documentation.
Good communication and interpersonal skills as parts of the work is done in cross functional teams
Good knowledge of standard Microsoft Office applications
Language skills in Swedish


Preferred requirements:
Experience from regulated business
It is also considered an advantage if you are familiar with ISO 13485:2016 Medical Device – Quality Management System and FDA Quality System Regulation 21 CFR Part 820 or have experience from medical device or other product areas with high regulatory demands.
Experience from manage measurement instruments, such as calipers, micrometers etc.


We look forward hearing from you, welcome with your application no later than October 8. Please note that we will review applications continuously, so be sure to send in your application as soon as possible.
Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona’s products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona’s global headquarters is located in Charlotte, North Carolina, USA. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY.
Bringing out the best in people
As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we’re looking for the best to join us.
Working at Dentsply Sirona you are able to:
Develop faster - with our commitment to the best professional development.
Perform better - as part of a high-performance, empowering culture.
Shape an industry - with a market leader that continues to drive innovation.
Make a difference -by helping improve oral health worldwide. Visa mindre

Har du erfarenhet av CNC och NC beredning och vill arbeta på ett medicintekniskt företag? Bli då en del av vårat team och vår häftiga produktionsmiljö.
Om rollen: I rollen kommer du att arbeta med produktion av tandimplantat där vi använder 7-axliga maskiner. Du kommer att arbeta med underhåll av programvara samt testning av verktyg. I arbetet ingår också att kunna läsa samt programmera iso-kod.
Vem är du? Vi ser att du är initiativrik, engagerad och noggrann som person. Du tar ansvar för ditt arbete och har vana av att kunna arbeta med små detaljer samt med hög precision. Vi lägger stor vikt vid din samarbetsförmåga då arbetet sker i en liten grupp.
Vi ser att du har:
teknisk utbildning på gymnasienivå eller likvärdig utbildning
CNC utbildning
praktisk erfarenhet av arbete med CNC maskiner

Datavana samt kunskaper i engelska (tal och skrift) ser vi som meriterande. Det är också meriterande om du har erfarenhet av:
att programmera ISO Kod
Fanuc Styrsystem
Autodesk Powermill
Parameter programmering
att mäta med mikrometer och Cmm (Mitutoyo mätmaskin)
ritningsläsning
verktygsdata

Bra att veta:Avdelningen Atlantis tillverkar individuellt anpassade distanser och försörjer Europamarknaden och Australien med Atlantis komponenter. Atlantis teknologi bygger på en unik metod som utgår från hur den färdiga tanden ska se ut. För att utveckla dessa komponenter används senaste CAD/CAM-teknologin. Verksamheten är kundorderstyrd med krav på utleverans till kund nästföljande dag.
För mer information, ring gärna rekryterande chef, Magnus Wolving, telefonnummer 0761-077947.
Ansökningar kommer att hanteras löpande, så skicka in din ansökan snarast möjligt.
Om Dentsply Sirona: Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona’s products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona’s global headquarters is located in Charlotte, North Carolina, USA. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY.
Bringing out the best in people
As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we’re looking for the best to join us. Visa mindre

Would you like to work in a context where you will make a real difference, where you can be creative and where your expertise counts? In this role you will combine science with commercial opportunities in a Health Economics context. Does this sound exciting?
The role resides with Global Medical Affairs, part of Global Marketing, at our headquarter in Mölndal/Gothenburg, Sweden. You will be responsible for the central management of health economics across therapy areas and products. Thorough understanding of commercial strategies and priorities is key. Your expertise is important to support ongoing business as well as new product development projects. You will have stakeholders and close collaborators across the organization, including local markets.
Responsibilities
To initiate and manage health economic projects.
To search for and analyze external data and scientific literature.
Reimbursement know-how and oversight.
Develop sales-/promotion-material to demonstrate the value of products, solutions and therapies.
To manage a relevant network of internal and external stakeholders.

Qualifications / Background
Relevant academic degree within Health Economics, preferably MSc or above.
It comes natural for you how to optimize health economic evidence to support business needs.
A background in similar roles within Medical Device is an advantage.
You have a proven commercial acumen.
You understand how health economic and clinical evidence are interlinked.
You are proficient in English (verbal and writing).
Swedish speaking is an advantage but not a prerequisite.

The preferred candidate has the drive, endurance and capability to set, and execute on goals and KPIs. You´re comfortable acting in cross functional teams as well as independently. You take initiatives, are creative and rise with a challenge. You have a positive attitude, and you are a strong communicator who is perceived as highly professional by peers and stakeholders.
We prefer you to be based at our headquarters in Mölndal/Gothenburg, but we are open for a remote position within Sweden for the right candidate.
We are interviewing candidates continuously, so to enhance your chances, we recommend that you send us your application as soon as possible.
Welcome with your application!
About Wellspect
Wellspect is a leading global provider of innovative medical devices that help people suffering from urinary retention or chronic constipation. More than 1 000 employees around the world are dedicated to making a difference to people who need our products and services. Wellspect is one of the worlds’ leading manufacturers of intermittent urinary catheters, with LoFric® as the most known brand. As a help to those with chronic or severe constipation Wellspect has developed what likely is the world’s most advanced irrigation system, Navina™, combining a high degree of user convenience, clinical effectiveness and connectivity into one smart system. Wellspect strives to become climate neutral and leave the smallest possible environmental footprint. The company, with headquarters in Mölndal, Sweden, is present in more than 30 countries, and part of Dentsply Sirona, the worlds´ largest manufacturer of professional dental technologies. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. Visit www.wellspect.com and www.dentsplysirona.com for more information. Visa mindre

Söker du utveckling inom drift och underhåll med möjlighet att utmana och utveckla våra högautomatiserade maskinanläggningar i Mölndal?
Om rollen.
I rollen kommer du att arbeta med underhåll inom vår produktionsanläggning som innefattar monterings-, bearbetnings- och förpackningsmaskiner samt en renings- och processanläggning där du kommer vara maskinansvarig för en maskin eller område.
Dina huvudsakliga arbetsuppgifter är;
driva förbättringsarbete på ditt område tillsammans med tvärfunktionell grupp som arbetar med utveckling av produkt och maskinområde
utveckling, testning, förbättring och driftsättning av nya och befintliga maskiner/processer tillsammans med andra avdelningar
driva arbete med att utveckla och förvalta förebyggande och avhjälpande underhåll för att bibehålla och säkerställa stabila processer på våra produktionsutrustningar

Vem är du
Vi ser att du är drivande och engagerad som person och vill vara med att förvalta och utveckla processer i en högautomatiserad produktionsmiljö tillsammans med dina kollegor i teamet
Vi ser att du har
dokumenterad teknisk kompetens och erfarenhet inom drift och underhåll
ett utmärkande kvalitets- och ett högt säkerhetstänkande
en kostnadsmedvetenhet med fokus på effektivt och långsiktigt underhåll
en hög kommunikativ förmåga, eftersom rollen innebär att du ska kunna kommunicera förtroendefullt, pedagogiskt och tydligt med personer på flera olika nivåer som har olika teknisk kunskap

Bra att veta
För mer information, ring gärna rekryterande chef, Mohammed Chkair, telefonnummer +46 31 376 45 61.
Ansökningar kommer att hanteras löpande, så skicka in din ansökan snarast möjligt.
Wellspect
Wellspect Healthcare är en ledande global leverantör av innovativ medicinsk utrustning som hjälper människor med blås- eller tarmdysfunktion. Wellspect har fler än 1000 anställda runt om i världen som dagligen bidrar till att göra skillnad för alla de människor som behöver företagets produkter och tjänster.
Wellspect är en världsledande tillverkare av intermittenta urinkatetrar, där LoFric® är det mest kända varumärket. Företaget har också utvecklat Navina™, en lösning som hjälper mot kronisk eller allvarlig förstoppning och avföringsläckage. Navina™ är förmodligen marknadens mest avancerade irrigationssystem, en smart digital lösning som kombinerar hög användarvänlighet med klinisk effektivitet.
Wellspect strävar efter att bli klimatneutralt med minsta möjliga påverkan på miljön. Företaget har sitt huvudkontor i Mölndal, är verksamt i över 30 länder och är en del av Dentsply Sirona –?världens största tillverkare av professionella dentala lösningar. Dentsply Sirona är listat på NASDAQ i USA under symbolen XRAY.
Besök www.wellspect.com eller www.dentsplysirona.com för mer information Visa mindre

Vill du vara med och driftsäkra våra högautomatiserade maskinanläggningar i Mölndal?
I rollen som Maintenance Technician kommer du att arbeta med underhåll inom vår produktionsanläggning som innefattar monterings-, bearbetnings- och förpackningsmaskiner samt en renings- och processanläggning.
Dina huvudsakliga arbetsuppgifter är;
Förebyggande och avhjälpande underhåll
Förbättringsarbete på våra högautomatiserade maskinanläggningar
Driftsättning, förbättring och testning av nya maskiner och processer tillsammans med andra avdelningar
Driftsäkring av vår produktionsanläggning

Vem är du
Vi ser att du är drivande som person och du tycker om att medverka i förbättringsarbete i en högautomatiserad produktionsmiljö. Du har en stor lust att lära dig nya saker och utvecklas i din roll.
Vi ser att du har
En gedigen dokumenterad teknisk kompetens inom drift och underhåll
Ett utmärkande kvalitetstänk och ett högt säkerhetstänk
En kostnadsmedvetenhet med fokus på effektivt och långsiktigt underhåll
En hög kommunikativ förmåga eftersom rollen innebär att du ska kunna kommunicera förtroendefullt, pedagogiskt och tydligt med personer på flera olika nivåer som har olika teknisk kunskap
Grundläggande PLC-kunskaper

Bra att veta
Arbetstiden är förlagd till kontinuerligt treskift.
För mer information, ring gärna rekryterande chef, Sebastian Brogren på telefonnummer +4670 227 79 34
Ansökningar kommer att hanteras löpande, så skicka gärna in din ansökan snarast möjligt.
Om Wellspect
Wellspect Healthcare är en ledande global leverantör av innovativ medicinsk utrustning som hjälper människor med blås- eller tarmdysfunktion. Wellspect har fler än 1000 anställda runt om i världen som dagligen bidrar till att göra skillnad för alla de människor som behöver företagets produkter och tjänster.
Wellspect är en världsledande tillverkare av intermittenta urinkatetrar, där LoFric® är det mest kända varumärket. Företaget har också utvecklat Navina™, en lösning som hjälper mot kronisk eller allvarlig förstoppning och avföringsläckage. Navina™ är förmodligen marknadens mest avancerade irrigationssystem, en smart digital lösning som kombinerar hög användarvänlighet med klinisk effektivitet.
Wellspect strävar efter att bli klimatneutralt med minsta möjliga påverkan på miljön. Företaget har sitt huvudkontor i Mölndal, är verksamt i över 30 länder och är en del av Dentsply Sirona –?världens största tillverkare av professionella dentala lösningar. Dentsply Sirona är listat på NASDAQ i USA under symbolen XRAY.
Besök www.wellspect.com eller www.dentsplysirona.com för mer information. Visa mindre

Sterilization Operator
Vill du vara med i en grupp som jobbar med ständiga förbättringar i en högautomatiserad anläggning?
Om rollen
Som steriloperatör ingår du i ett skiftlag som arbetar kontinuerligt 3-skift. Tillsammans med dina kollegor sköter ni den dagliga driften av vår strålsteriliseringsprocess. Vi steriliserar det som tillverkas i fabriken med hjälp av joniserad strålning.
I ditt ansvarsområde ingår:
Övervakning av steriliseringsprocessen
Förebyggande och avhjälpande underhåll
Godshantering/Pallhantering
Mätning och verifiering av produktionsparametrar
Administration
Förbättringsarbete
Rapportering i olika elektroniska system

Vem är du
En självgående person som har en teknisk utbildning eller en erfarenhet som bedöms likvärdig. Arbetet kräver att du är ansvarstagande och noggrann.
Vi ser att du har:
God samarbetsförmåga då man dagligen kommunicerar med andra avdelningar och mycket av arbetet sker i små grupper
Högt säkerhets- och kvalitetstänkande
En teknisk förståelse och ett praktiskt handlag då underhåll är en stor del av arbetet.
God datavana, då vi hanterar det mesta via styrsystem och elektroniska rapporteringar.
Kan uttrycka dig väl i tal och skrift samt förstå instruktioner och dokumentation skriven på svenska

Bra att veta
För mer information, ring gärna rekryterande chef, Stefan Giza, telefonnummer 0702-59 28 53
Ansökningar kommer att hanteras löpande, så skicka gärna in din ansökan snarast möjligt.
Wellspect
Wellspect Healthcare är en ledande global leverantör av innovativ medicinsk utrustning som hjälper människor med blås- eller tarmdysfunktion. Wellspect har fler än 1000 anställda runt om i världen som dagligen bidrar till att göra skillnad för alla de människor som behöver företagets produkter och tjänster.
Wellspect är en världsledande tillverkare av intermittenta urinkatetrar, där LoFric® är det mest kända varumärket. Företaget har också utvecklat Navina™, en lösning som hjälper mot kronisk eller allvarlig förstoppning och avföringsläckage. Navina™ är förmodligen marknadens mest avancerade irrigationssystem, en smart digital lösning som kombinerar hög användarvänlighet med klinisk effektivitet.
Wellspect strävar efter att bli klimatneutralt med minsta möjliga påverkan på miljön. Företaget har sitt huvudkontor i Mölndal, är verksamt i över 30 länder och är en del av Dentsply Sirona –?världens största tillverkare av professionella dentala lösningar. Dentsply Sirona är listat på NASDAQ i USA under symbolen XRAY.
Besök www.wellspect.com eller www.dentsplysirona.com för mer information. Visa mindre

Come join our dynamic team in a role where you will work with many different tasks and be able get insight in and learn more about quality and regulatory. We are a global company where you can really make a difference.
Don´t miss this opportunity!
Responsibilities:
coordinate larger meetings within Quality/Regulatory Department
prepare agendas
note taking
distributions of meeting minutes
follow-up activities as needed
maintenance of Document Templates and Lists
general system/database administration
statistic collecting and reporting
supporting vigilance general monitoring
supporting external audits
supporting product registrations and tenders

Qualification / Background
Experience from similar tasks in a coordinator or administrative role
Well experienced in working with general Office package, specifically in One-Note, Sharepoint and Teams specifically
Comfortable in using English and Swedish language
Experience from work within Medical Devices company is desirable

In this role you will work with a lot of different tasks and contact settings. You will need to be service minded and flexible with a drive to take ownership and initiatives. We are looking for someone that is structured and well organized. It is also important that you are a team player.
Please note that we will review applications continuously, so be sure to send in your application as soon as possible. Please send us your application English.
We look forward hearing from you.
About Wellspect
Wellspect is a leading global provider of innovative medical devices that help people suffering from urinary retention or chronic constipation. More than 1 000 employees around the world are dedicated to making a difference to people who need our products and services. Wellspect is one of the worlds’ leading manufacturers of intermittent urinary catheters, with LoFric® as the most known brand. As a help to those with chronic or severe constipation Wellspect has developed what likely is the world’s most advanced irrigation system, Navina™, combining a high degree of user convenience, clinical effectiveness and connectivity into one smart system. Wellspect strives to become climate neutral and leave the smallest possible environmental footprint. The company, with headquarters in Mölndal, Sweden, is present in more than 30 countries, and part of Dentsply Sirona, the worlds´ largest manufacturer of professional dental technologies. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. Visit www.wellspect.com and www.dentsplysirona.com for more information. Visa mindre

Vill du vara med och driftsäkra våra högautomatiserade maskinanläggningar i Mölndal?
I rollen som Maintenance Technician kommer du att arbeta med underhåll inom vår produktionsanläggning som innefattar monterings-, bearbetnings- och förpackningsmaskiner samt en renings- och processanläggning.
Dina huvudsakliga arbetsuppgifter är;
Förebyggande och avhjälpande underhåll
Förbättringsarbete på våra högautomatiserade maskinanläggningar
Driftsättning, förbättring och testning av nya maskiner och processer tillsammans med andra avdelningar
Driftsäkring av vår produktionsanläggning

Vem är du
Vi ser att du är drivande som person och du tycker om att medverka i förbättringsarbete i en högautomatiserad produktionsmiljö. Du har en stor lust att lära dig nya saker och utvecklas i din roll.
Vi ser att du har
En gedigen dokumenterad teknisk kompetens inom drift och underhåll
Ett utmärkande kvalitetstänk och ett högt säkerhetstänk
En kostnadsmedvetenhet med fokus på effektivt och långsiktigt underhåll
En hög kommunikativ förmåga eftersom rollen innebär att du ska kunna kommunicera förtroendefullt, pedagogiskt och tydligt med personer på flera olika nivåer som har olika teknisk kunskap
Grundläggande PLC-kunskaper

Bra att veta
Arbetstiden är förlagd till kontinuerligt treskift.
För mer information, ring gärna rekryterande chef, Sebastian Brogren på telefonnummer +4670 227 79 34
Ansökningar kommer att hanteras löpande, så skicka gärna in din ansökan snarast möjligt.
Om Wellspect
Wellspect Healthcare är en ledande global leverantör av innovativ medicinsk utrustning som hjälper människor med blås- eller tarmdysfunktion. Wellspect har fler än 1000 anställda runt om i världen som dagligen bidrar till att göra skillnad för alla de människor som behöver företagets produkter och tjänster.
Wellspect är en världsledande tillverkare av intermittenta urinkatetrar, där LoFric® är det mest kända varumärket. Företaget har också utvecklat Navina™, en lösning som hjälper mot kronisk eller allvarlig förstoppning och avföringsläckage. Navina™ är förmodligen marknadens mest avancerade irrigationssystem, en smart digital lösning som kombinerar hög användarvänlighet med klinisk effektivitet.
Wellspect strävar efter att bli klimatneutralt med minsta möjliga påverkan på miljön. Företaget har sitt huvudkontor i Mölndal, är verksamt i över 30 länder och är en del av Dentsply Sirona –?världens största tillverkare av professionella dentala lösningar. Dentsply Sirona är listat på NASDAQ i USA under symbolen XRAY.
Besök www.wellspect.com eller www.dentsplysirona.com för mer information. Visa mindre

Inom avdelningen Produktionsteknik kommer du tillsammans med inspirerande kollegor att hitta nya vägar att kontinuerligt förbättra vår produktion.
Om tjänsten Som produktionstekniker ansvarar du för att:
Utveckla standardiserade arbetssätt
Utbildningar i arbetssätt och metoder
Delta i förbättringsarbete
Stötta organisationen I LEAN-arbete genom att aktivt coacha operatörer
Tillse att 5S efterlevs
Planera underhåll och koordinera detta tillsammans med underhållsavdelningen
Planera och boka in kalibreringar
Köpa in verktyg och utrustning för bl.a. materialhantering
Delta i tvärfunktionell grupp
Delta i projekt tillsammans med andra avdelningar inom operations

Vem är du Vi söker dig som vill arbeta tillsammans med kompetenta och engagerade kollegor som tillsammans vill göra skillnad.
Vi söker dig som:
Har gymnasial utbildning
Uppskattar att arbeta med människor och är bra på kommunikation
Arbetat i produktion, såsom, operatör, kvalitetsarbete, underhåll och produktionsadministration
Har goda kunskaper inom produktionsteknik och underhållsteknik
Arbetat med Lean som ett standardiserande arbetssätt.
Är ansvarstagande, lösningsinriktad och har en förmåga att skapa ordning och reda.
Kan uttrycka dig väl i tal och skrift på Svenska, då kommunikation och utbildning av personal sker på svenska.

Bra att veta För mer information, kontakta gärna rekryterande chef, Anna Eriksson, 070-384 38 36, [email protected]
Ansökningar kommer att hanteras löpande, så skicka in din ansökan snarast möjligt. Visa mindre

Om rollen I rollen som Spare Part Technician kommer du att arbeta med registrering, inköp och lagerhantering av reservdelar till våra produktionsmaskiner.
Dina huvudsakliga arbetsuppgifter är;
Att administrera reservdelshanteringen i vårt underhållssystem.
Att tillsammans med kollegor på avdelning registrera nya reservdelar där behov finns.
Vid behov lägga beställning på reservdelar samt bevaka leveransen.
Vid behov söka nya leverantörer tillsammans med Inköpare.
Att arbeta med förbättringsarbete inom eget arbetsområde samt stödja andra förbättringsgrupper.


Vem du är Vi tror att du har minst tre års erfarenhet av liknande arbetsuppgifter. Du är en noggrann, strukturerad och serviceinriktad person som tar ansvar för ditt arbete. Du motiveras av att ta initiativ och samarbetar gärna tillsammans med engagerade kollegor men kan också arbeta individuellt.
Vi tror att du har;
Gymnasieexamen.
Goda kunskaper i engelska såväl i tal som skrift.
Vana att arbeta i datoriserade system.


Bra att veta Detta är en tjänst för tillsvidareanställning med arbetstid förlagd till dagtid.
För mer information, vänligen kontakta rekryterande chef, Patrik Brahm, telefonnummer, 031-376 33 60.
Sista ansökningsdagen är 23 december.
Dentsply Sirona Dentsply Sirona är världens största tillverkare av tandvårdsprodukter och -lösningar, och har under 130 år erbjudit innovationer och service till tandvårdssektorn och patienter över hela världen. Dentsply Sirona utvecklar, tillverkar och marknadsför ett heltäckande utbud av produkter och lösningar för dental hälsa, liksom andra medicintekniska förbrukningsartiklar och har en stark varumärkesportfölj i världsklass. Dentsply Sirona marknadsför innovativa, högkvalitativa och effektiva lösningar för avancerad patientvård som ger bättre och säkrare tandvård. Dentsply Sironas globala huvudkontor ligger i Charlotte, North Carolina, USA. Företagets aktier är listade på amerikanska NASDAQ under symbolen XRAY. Visa mindre

Vill du dela en stark passion för att göra skillnad, en verklig skillnad, för våra användare, våra kunder och för samhället i stort?
Som en av våra Warehouse Worker’s inom Promotion kommer du att arbeta inom den nordiska säljorganisationen och vara en del av vårt centrala nordiska marknads- och kundserviceteam i Mölndal.
Om rollen I rollen kommer du arbeta med att stödja de nordiska marknaderna med leveranser av marknadsmaterial, produktprover, kongressmaterial, utbildningsmaterial mm, både internt och externt. Du kommer arbeta nära flera olika kontakter såsom vår nordiska säljorganisation, marknads- och kundservicekoordinatorer, leverantörer och transportörer.
Arbetstiden är förlagd till dagtid.
Dina huvudsakliga arbetsuppgifter är
Orderhantering – plock, pack och rapportering
Ansvara för in/utleveranser
Beställning packmaterial, förbrukningsmaterial, produkter, marknadsmaterial


Vem är du Vi tror att du är en serviceinriktad, kvalitetsmedveten, flexibel och noggrann person som tar stort ansvar för ditt arbete. Du tycker om att ta egna initiativ och samarbetar gärna tillsammans med engagerade kollegor men kan också arbeta självständigt.
Vi vill att du har
Gymnasieutbildning
Erfarenhet från lagerarbete
Truckkort
Datavana (word/excel)
Engelska i tal och skrift
Har en förståelse för norska och danska språket

Det är meriterande om du har erfarenhet av orderhantering och M3.
Ansökningar kommer att hanteras löpande, så skicka in din ansökan snarast möjligt.
Wellspect HealthCare Wellspect Healthcare is a leading global provider of innovative medical devices that help people suffering from urinary retention or chronic constipation. More than 1 000 employees around the world are dedicated to making a difference to people who need our products and services. Wellspect is one of the worlds’ leading manufacturers of intermittent urinary catheters, with LoFric® as the most known brand. As a help to those with chronic or severe constipation Wellspect has developed what likely is the world’s most advanced irrigation system, Navina™, combining a high degree of user convenience, clinical effectiveness and connectivity into one smart system. Wellspect strives to become climate neutral and leave the smallest possible environmental footprint. The company, with headquarters in Mölndal, Sweden, is present in more than 30 countries, and part of Dentsply Sirona, the worlds´ largest manufacturer of professional dental technologies. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. Visit www.wellspect.com and www.dentsplysirona.com for more information. Visa mindre

Om rollen I rollen som Machine Operator kommer du att sköta våra 3D printers, Pvd beläggningsmaskiner, lasersvets samt sköta vår sorteringsstation där vi hanterar alla våra produkter för vidare leverans ut.
Dina huvudsakliga arbetsuppgifter är:
Att svetsa
Att rapportera material
Att kontrollera distanser och köra dem i vår beläggningsprocess
Att ladda in filer, ta ut guider samt rengöra 3D printrar


Vem är du Vi tror att du är en ordningsam person som tar ansvar för sitt arbete. Du samarbetar gärna med dina engagerade kollegor men kan också arbeta individuellt.
För att trivas i rollen tror vi att du har:
Datorvana
Bra sifferminne då det underlättar arbete med rapportering
Tekniskt intresse
Noggrannhet för att säkerställa kvaliteten av produkterna


Bra att veta Detta är en tjänst för tillsvidareanställning.
För mer information, ring gärna rekryterande chef, Bengt Otterdahl, telefonnummer: 031 - 3764496.
Sista ansökningsdag är den 11 september. Ansökningar kommer att hanteras löpande, så skicka in din ansökan snarast möjligt. Visa mindre

Do you want to be a part of a team that works with material and production planning of products that make a real difference every day for our customers?
About the position You will be responsible for planning a part of our assortment of finished products and raw materials. Delivery precision is our primary target, but also balance with inventory levels and production capacity. The planning is both on tactical level (monthly and weekly production pace, delivery plan to suppliers) as well as daily production planning and purchase orders. The work involves also evaluation of sales forecast from our markets.
Your key responsibilities are:
Raw material planning
Handling of supplier deviations
Production planning
Follow up on production, inventory levels and deliveries
Set weekly targets for production
Participate in cross-functional teams and projects



Who you are We think you are a structured person who likes problem solving. You like to work in a dynamic environment and to handle changes.
We believe you have:
A few years of planning or operative purchasing or similar from a manufacturing company
Experience from working in an ERP system
Good knowledge of MS Office
Basics knowledge of LEAN production principles
Strong communication skills in both English and Swedish



Good to know Please note that we will review applications continuously, so be sure to send in your application as soon as possible.
About Wellspect HealthCare Wellspect Healthcare, with headquarters in Mölndal, Sweden, is a leading global provider of innovative medical devices with a focus on helping people suffering from urinary retention or chronic constipation. Every day, more than 1 100 employees are dedicated to make a difference for those who need our products and services. Many of the people we serve have a spinal cord injury, enlarged prostate, spina bifida or multiple sclerosis. We are one of the world’s leading manufacturers of intermittent urinary catheters, with LoFric® as our most known brand. As a help to those with chronic or severe constipation we have developed what likely is the world’s most advanced irrigation system, the Navina Systems™, combining a high degree of user convenience, clinical effectiveness and connectivity into one really smart system. Wellspect HealthCare has a presence in more than 30 countries, and is a part of Dentsply Sirona, the worlds´ largest manufacturer of professional dental products and technologies with headquarters in Charlotte, North Carolina, USA. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. Visit www.wellspect.com and www.dentsplysirona.com for more information. Visa mindre

Bli en del av vårt härliga team som arbetar med individuellt anpassade distanser med en teknologi som bygger på en unik process.
Om rollen I rollen som Abutment Design Technician designar du kundspecifika distanser och kronor i ett egenutvecklat CAD system. Verksamheten är kundorderstyrd med krav på utleverans till kund nästföljande dag. I dina arbetsuppgifter ingår;
Att designa utefter kundorder
Kvalitetskontroll och att frisläppa tillverknings order
Att ha kontakt med kunder för att lösa specifika kundkrav
Att arbeta med LEAN-konceptet för att kontinuerlig utveckling av vår verksamhet



Vem du är Vi tror att du är en kvalitetsmedveten och noggrann person som gillar att tillhandahålla god service gentemot kunder. Du är öppen för nya utmaningar och vill arbeta tillsammans med engagerade kollegor där varje dag gör skillnad.
Vi tror att du har;
Tandteknisk utbildning och gärna med erfarenhet av tandtekniskt laboratorium
God datorvana och känner dig bekväm i en helt digital miljö
Vana av att analysera och ta beslut
Motivation och trivs med att arbeta såväl självständigt som i grupp
Goda kunskaper i engelska, ytterligare språkkunskaper är meriterande



Bra att veta Vår förhoppning är att tillsätta denna roll snarast möjligt, men vi föredrar att hitta rätt person än att hitta någon snabbt.
Anställningsform: Tillsvidare
För mer information, vänligen kontakta rekryterande chef, Erik Carlsson, telefonnummer 0702-29 43 29.
Sista ansökningsdagen är 25:e September, 2022. Ansökningar kommer att hanteras löpande så skicka in din ansökan snarast möjligt
Om Dentsply Sirona Dentsply Sirona är världens största tillverkare av tandvårdsprodukter och -lösningar, och har under 130 år erbjudit innovationer och service till tandvårdssektorn och patienter över hela världen. Dentsply Sirona utvecklar, tillverkar och marknadsför ett heltäckande utbud av produkter och lösningar för dental hälsa, liksom andra medicintekniska förbrukningsartiklar och har en stark varumärkesportfölj i världsklass. Som ”The Dental Solutions Company”, marknadsförs innovativa, högkvalitativa och effektiva lösningar för avancerad patientvård som ger bättre, säkrare och snabbare behandling. Dentsply Sironas globala huvudkontor ligger i USA, i Charlotte, North Carolina, och det internationella huvudkontoret finns i Salzburg, Österrike. Företagets aktier är listade på amerikanska NASDAQ under symbolen XRAY. Mer information om Dentsply Sirona och dess produkter finns på www.dentsplysirona.com. Visa mindre

Service minded person to work with distribution in an international environment.
About the position As Customer Order Coordinator you will work in the Supply Chain department where you will be one of two customer order coordinators.
High service level to our customers is most important for us. You will handle urgent matters as well as work proactive and in a structured way to secure our deliveries. In this role you will work closely with a lot of different contacts such as, customers, our sales companies worldwide, our warehouses, Finance, transport companies and also with colleagues within Supply Chain.
Your key responsibilities are
Customer Order Administration
Customer Service for our export customers and sales companies
Manage shipment to our export customers and Wellspect warehouses worldwide
Arrange and follow up Transports
Document handling for Customs and Export
Manage Transport Invoices

Who you are We think you are service minded and like to have a lot of different tasks during the day. You are used to take your own initiatives and can identify potential problems, find solutions and take appropriate actions. Since you will work with a lot of different contacts, strong communication and collaboration skills are important.
We believe you have
A few years of customer service experience or similar from a manufacturing and/or distribution company
Knowledge of export documentation and Letter of credit
Good knowledge of MS Office
Experience from working in an ERP system
Strong communication skills in both English and Swedish

Good to know Please note that we will review applications continuously, so be sure to send in your application as soon as possible.
About Wellspect Wellspect is a leading global provider of innovative medical devices that help people suffering from urinary retention or chronic constipation. More than 1 000 employees around the world are dedicated to making a difference to people who need our products and services. Wellspect is one of the worlds’ leading manufacturers of intermittent urinary catheters, with LoFric® as the most known brand. As a help to those with chronic or severe constipation Wellspect has developed what likely is the world’s most advanced irrigation system, Navina™, combining a high degree of user convenience, clinical effectiveness and connectivity into one smart system. Wellspect strives to become climate neutral and leave the smallest possible environmental footprint. The company, with headquarters in Mölndal, Sweden, is present in more than 30 countries, and part of Dentsply Sirona, the worlds´ largest manufacturer of professional dental technologies. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. Visit www.wellspect.com for more information. Visa mindre

Vill du vara med och driftsäkra våra högautomatiserade maskinanläggningar i Mölndal?
Om rollen I rollen som Maintenance Engineer kommer du att vara med och utveckla och förbättra vår produktionsanläggning som innefattar bearbetnings- och förpackningsmaskiner samt E-beam steriliseringsanläggning. Här ges det möjlighet att lära sig tekniken i vår steriliseringsanläggning.
Dina huvudsakliga arbetsuppgifter är;
problemlösning för att driftsäkra och supporta vår E-beam steriliseingsanläggning
ta fram förbättrings- och konceptlösningar för att utveckla våra maskinanläggningar
delta i projekt för driftsättning av ny utrustning
delta i projekt för att säkerställa driftsäkerhet vid industrialisering av nya produkter
genom ständiga förbättringar utveckla och effektivisera vårt underhållsarbete
hålla hög kompetens inom den senaste tekniken

Vem är du Vi ser att du är drivande som person och du tycker om att medverka i förbättringsarbete i en högautomatiserad produktionsmiljö.
Vi ser att du har:
God kunskap inom felsökning på elektronik
Erfarenhet från arbete som exempelvis servicetekniker, serviceingenjör, installatör eller elektriker
teknisk kompetens inom drift och underhåll
ett utmärkande kvalitetstänkande och ett högt säkerhetstänkande
en kostnadsmedvetenhet med fokus på effektivt och långsiktigt underhåll
en hög kommunikativ förmåga, eftersom rollen innebär att du ska kunna kommunicera förtroendefullt, pedagogiskt och tydligt med personer på flera olika nivåer som har olika teknisk kunskap

För mer information, ring gärna rekryterande chef, Markus Jansson, telefonnummer +46 31 376 4642.
Sista ansökningsdagen är 31 januari. Ansökningar kommer att hanteras löpande, så skicka in din ansökan snarast möjligt.
Om Wellspect Wellspect Healthcare är en ledande global leverantör av innovativ medicinsk utrustning som hjälper människor med blås- eller tarmdysfunktion. Wellspect har fler än 1000 anställda runt om i världen som dagligen bidrar till att göra skillnad för alla de människor som behöver företagets produkter och tjänster.
Wellspect är en världsledande tillverkare av intermittenta urinkatetrar, där LoFric® är det mest kända varumärket. Företaget har också utvecklat Navina™, en lösning som hjälper mot kronisk eller allvarlig förstoppning och avföringsläckage. Navina™ är förmodligen marknadens mest avancerade irrigationssystem, en smart digital lösning som kombinerar hög användarvänlighet med klinisk effektivitet.
Wellspect strävar efter att bli klimatneutralt med minsta möjliga påverkan på miljön. Företaget har sitt huvudkontor i Mölndal, är verksamt i över 30 länder och är en del av Dentsply Sirona –?världens största tillverkare av professionella dentala lösningar. Dentsply Sirona är listat på NASDAQ i USA under symbolen XRAY.
Besök www.wellspect.com eller www.dentsplysirona.com för mer information. Visa mindre

Söker du utveckling inom drift och underhåll med möjlighet att utmana och utveckla våra högautomatiserade maskinanläggningar i Mölndal?
Vi kommer under året starta ytterligare högautomatiserade maskinanläggningar i vår produktion i Mölndal och vi behöver därför utöka vår grupp med ytterligare en Maintenance and Operating Technician.
Om rollen. I rollen kommer du att arbeta med underhåll inom vår produktionsanläggning som innefattar monterings-, bearbetnings- och förpackningsmaskiner samt en renings- och processanläggning där du kommer vara maskinansvarig för en maskin eller område.
Dina huvudsakliga arbetsuppgifter är;
driva förbättringsarbete på ditt område tillsammans med tvärfunktionell grupp som arbetar med utveckling av produkt och maskinområde
utveckling, testning, förbättring och driftsättning av nya och befintliga maskiner/processer tillsammans med andra avdelningar
driva arbete med att utveckla och förvalta förebyggande och avhjälpande underhåll för att bibehålla och säkerställa stabila processer på våra produktionsutrustningar

Vem är du Vi ser att du är drivande och engagerad som person och vill vara med att förvalta och utveckla processer i en högautomatiserad produktionsmiljö tillsammans med dina kollegor i teamet
Vi ser att du har
dokumenterad teknisk kompetens och erfarenhet inom drift och underhåll
ett utmärkande kvalitets- och ett högt säkerhetstänkande
en kostnadsmedvetenhet med fokus på effektivt och långsiktigt underhåll
en hög kommunikativ förmåga, eftersom rollen innebär att du ska kunna kommunicera förtroendefullt, pedagogiskt och tydligt med personer på flera olika nivåer som har olika teknisk kunskap

Bra att veta För mer information, ring gärna rekryterande chef, Markus Kristiansson, telefonnummer +46 31 376 33 26.
Ansökningar kommer att hanteras löpande, så skicka in din ansökan snarast möjligt.
Om Wellspect HealthCare Wellspect HealthCare, med huvudkontor i Mölndal i Sverige, är en ledande global leverantör av innovativa medicintekniska produkter och tjänster med fokus på hjälpa människor som lider av urinretention eller kronisk förstoppning. Varje dag arbetar mer än 1 100 engagerade medarbetare med att göra skillnad för de som behöver våra produkter och våra tjänster. Många av dem som vi hjälper har ryggmärgsskada, förstorad prostata, ryggmärgsbråck eller multipel skleros. Vi är en av världens ledande tillverkare av intermittenta urinkatetrar, med LoFric® som vårt mest kända varumärke. Som hjälp till de med kronisk eller svår förstoppning har vi utvecklat vad som sannolikt är världens mest avancerade irrigationssystem, Navina Systems™, vilket kombinerar en hög grad av användarvänlighet, klinisk effekt och kommunikation i ett verkligt smart system. Wellspect HealthCare är representerat i fler än 30 länder samt ingår i Dentsply Sirona, världens största tillverkare av professionella tandvårdsprodukter och teknologier med huvudkontor i North Carolina, USA. Företagets aktier är listade på amerikanska NASDAQ under symbolen XRAY. Mer information finns på www.wellspect.com och www.denstplysirona.com. Visa mindre

Do you want to join our team working in a truly global environment?

In this role you will be a key contributor using your expertise in our research and development projects of medical devices across our different platforms, Implants, Regenerative and Digital Solutions. You will collaborate with some of the sharpest expert in the industry in a role where you will use both your hands-on expertise as well as your theoretical mind.

Responsibilities:
Planning, execution and documentation of testing and analyses in product development projects and identified product changes
Development and validation of suitable test methods
Contribution to the process of building and establishing the laboratory service function to meet requests from different R&D platforms
Maintain and develop laboratory facilities and equipment to meet current and future requirements


We think you are a positive, proactive and driven team player with hands-on and can-do-attitude. In a regulated laboratory environment, you are good at using creative and innovative thinking to solve problems and improve existing processes. You are open for challenges and enjoy working together with highly skilled and committed colleagues where every day makes a difference.

Background / Qualifications:
An academic background, preferably in Mechanical Engineering, Material Science or equivalent with several years of experience in the field of medical device development
Experience in operating and troubleshooting mechanical equipment in a lab environment and analyzing the results
In depth knowledge of statistics and data analyzing skills and the ability to present data
Passion to provide accurate data with attention to detail
Analytical skills, scientific and innovative thinking and a proactive approach combined with a high level of personal accountability and accuracy
Excellent documentation and communication skills, in English as well as Swedish


The position is situated at the Dentsply Sirona Implants headquarter in Mölndal, Sweden.

For more information, please contact recruiting manager, Florian Tebbel, +49 625116 3803.

Welcome with your application no later than December 5th, 2021. Please note that we will review applications continuously, so be sure to send in your application as soon as possible.

We look forward hearing from you! Visa mindre

Join our Production Development team and continue shaping medical device production systems of tomorrow.
As a Production Development Engineer - Process you will play a key role in the development and implementation of new and improved production processes at Wellspect. In this role you will interact with various stakeholders to understand how products are configured as well as the requirements for efficient production flows. We are proud to have an in-house, highly automated medical device production with interconnected coating and media processes and multiple transport systems and packaging machines. And as a leading medical device manufacturer we have strict requirements on traceability and applications using in-line quality control.
Responsibilities;
Process project management in cross-functional development projects in various stages from concept to commissioning and handover.
Process design of media systems and applications, including e.g. pipes, pumps, valves, instruments and other production related equipment, as well as installation procedures.
Process risk assessment and User Requirements, functional and technical specifications
Commissioning and validation and training of operators
Develop documentation in compliance with our quality management system built on regulatory requirements from the European medical device directive and FDA quality systems regulations.
Integration of process equipment and components with a systems perspective on process control, traceability and communication with MES/SCADA and other production systems and equipment.
Establish and maintain working relationships with supplier including evaluations and supplier visits.


We think you are a positive, systematic and driven team player. You are open for challenges and enjoy working together with highly skilled and committed colleagues.
Qualifications / Background
an academic background, preferably in chemical or mechanical engineering or equivalent
experience in process design with focus on process media applications
an in-depth understanding process design including P&ID;.
experience from working with technical specifications and external suppliers
technical project management experience
experience from testing/validation, preferably within life science or other highly regulated industry
knowledge of GMP
knowledge aseptic and CIP/SIP design is to be considered a plus
documentation and communication skills, in English as well as in Swedish


Wellspects’ production is in continuous evolvement and there are always new and interesting projects going on. We offer you a place to develop your skills as part of a cross-functional team and the medical devices we manufacture make a real difference in the lives of our users. That’s a reason to go to work!
For more information, please contact recruiting manager, Anders Fagerström, telephone +46 31 376 33 73.
Please apply no later than November 14th , 2021. Please note that we will review applications continuously, so be sure to send in your application as soon as possible. Visa mindre

Join our Production Development team and continue shaping medical device production of tomorrow.

As a Process Manager you will be responsible for one or more production lines and together with a cross-functional team secure that the processes consistently and efficiently are able to deliver high quality products. You and your cross-functional team will continuously improve the production process and eliminate root causes regarding e.g. technical failures and non-conforming products.

Wellspect is proud to have an in-house, highly automated medical device production. We have strict requirements on traceability and in-line quality control; an area where we apply Big Data principles. The data collection and the ongoing initiatives to further facilitate analysis and visualization of the data give the Process Manager and the rest of the team great possibilities to analyze data and suggest and perform improvements.

Responsibilities:
To be responsible for the change control within your area, including continuous process risk management and maintaining the validated state of the equipment.
To lead a cross-functional coordination team from different departments.
To support the Manufacturing organization in technical issues and identify areas where technical improvements are possible and/or necessary.
To be involved when new or significantly changed products are affecting your process area, e.g. during the early stage of the project when the requirements are set and during planning and completion of the final stages with validation, launch and ramp-up.


We think you are a structured problem solver and efficient communicator. You also have an interest in bringing the best out of people and processes.

Qualifications / Background:
proven leaderships skills in leading teams and experience in driving changes
an academic background, preferably in automation/electrical/mechanical engineering or equivalent with experience from production development
extensive knowledge of automated manufacturing process
knowledge of Lean production concepts and experience from DMAIC and/or other Six Sigma methodologies
experience from working with technical specifications and change control
some experience from testing/validation, preferably within life science or other regulated industry
documentation and communication skills in Swedish and English
it is also an advantage if you have experience from polymer technology.


For more information, contact recruiting manager, Kristina Kull Österlin, telephone +46 31 376 32 49.
Welcome with your application. Please note that we will review applications continuously, so be sure to send in your application as soon as possible.

We look forward hearing from you! Visa mindre

Vill du vara med i en grupp som jobbar med ständiga förbättringar i en högautomatiserad anläggning?
Om rollen
Som steriloperatör ingår du i ett skiftlag som arbetar kontinuerligt 3-skift. Tillsammans med dina kollegor sköter ni den dagliga driften av vår strålsteriliseringsprocess. Vi steriliserar det som tillverkas i fabriken med hjälp av joniserad strålning.
I ditt ansvarsområde ingår:
Övervakning av steriliseringsprocessen
Förebyggande och avhjälpande underhåll
Godshantering/Pallhantering
Mätning och verifiering av produktionsparametrar
Administration
Förbättringsarbete
Rapportering i olika elektroniska system



Vem är du
En självgående person som har en teknisk utbildning eller en erfarenhet som bedöms likvärdig. Arbetet kräver att du är ansvarstagande och noggrann.
Vi ser att du har:
God samarbetsförmåga då man dagligen kommunicerar med andra avdelningar och mycket av arbetet sker i små grupper
Högt säkerhets- och kvalitetstänkande
En teknisk förståelse och ett praktiskt handlag då underhåll är en stor del av arbetet.
God datavana, då vi hanterar det mesta via styrsystem och elektroniska rapporteringar.
Kan uttrycka dig väl i tal och skrift samt förstå instruktioner och dokumentation skriven på svenska


Bra att veta
För mer information, ring gärna rekryterande chef, Stefan Giza, telefonnummer 0702-59 28 53
Ansökningar kommer att hanteras löpande, så skicka gärna in din ansökan snarast möjligt.
Om Wellspect HealthCare
Wellspect HealthCare, med huvudkontor i Mölndal i Sverige, är en ledande global leverantör av innovativa medicintekniska produkter och tjänster med fokus på att hjälpa människor som lider av urinretention eller kronisk förstoppning. Varje dag arbetar mer än 1 100 engagerade medarbetare med att göra skillnad för de som behöver våra produkter och våra tjänster. Många av dem som vi hjälper har ryggmärgsskada, förstorad prostata, ryggmärgsbråck eller multipel skleros. Vi är en av världens ledande tillverkare av intermittenta urinkatetrar, med LoFric® som vårt mest kända varumärke. Som hjälp till de med kronisk eller svår förstoppning har vi utvecklat vad som sannolikt är världens mest avancerade irrigationssystem, Navina Systems™, vilket kombinerar en hög grad av användarvänlighet, klinisk effekt och kommunikation i ett verkligt smart system. Wellspect HealthCare är representerat i fler än 30 länder samt ingår i Dentsply Sirona, världens största tillverkare av professionella tandvårdsprodukter och teknologier med globalt huvudkontor i Charlotte, North Carolina i USA. Företagets aktier är listade på amerikanska NASDAQ under symbolen XRAY. Mer information finns på www.wellspect.com och www.denstplysirona.com. Visa mindre

A great opportunity for you who wants to work as Project Manager with products that make a real difference.
As Project Manager at Wellspect Healthcare, you will be the tactical and operational team leader with complete ownership of project results, agile pacing, resource balancing and financial control of the projects within Wellspects New Product Introduction portfolio. You will plan, organize, lead and control projects to ensure on-time and qualitative delivery within the projects. Our recently launched strategy will also enable opportunities for you to potentially lead change and improvement projects.
You will become part of a team where we challenge and explore new ways of working, in our effort to continuously improve ourselves, individually and as a team. Our team culture is characterized by open and supportive attitudes andtogether we are moving our product portfolio to the next stages.
Responsibilities
Leading projects in compliance with corporate policies, quality and management systems within Wellspect, existing laws and regulations as well as standards and agreements.
Planning, organizing, directing and controlling projects according to company development process
Lead development projects for new products and upcoming generations
Continuously improve our project working procedures according to Lean Product Development principles


We think you are a positive team player with holistic view that enjoy creating result. You are open for challenges and enjoy working together with highly skilled and committed colleagues. To be successful in this role you are motivated by developing and driving projects forward and enjoy reaching goals as a team. Planning and organizing is something that comes naturally to you and you thrive in a coaching/leading position.
Qualifications / Background
An academic background
Extensive experience from working with product development in a project leading position
You can also have a background as management consultant
It´s an advantage if you have experience from working as a line manager in a technical product environment or complex environment
As documentation is a big part of the job, excellent communication skills in English and Swedish, both oral and written are essential


This position is located at our headquarter in Mölndal, Sweden
For more information, please contact Anders Tennby, recruiting manager and Head of Project Portfolio Management, phone 031-376 44 02.
Please apply no later than October 24th, 2021. Please note that we will review applications continuously. Visa mindre

Come join us in a strategically significant role partnering with Senior and Executive Leaders as a Financial Planning Analyst (FP&A). Do you enjoy working with numbers and analyzing & interpreting data? Are you motivated by data driven strategic decision making? Are you a proactive, data passionate, and intellectually curious analyst, with excellent written and oral communication skills? If you are looking for professional growth and an opportunity to showcase your talent with an international organization, do not miss this opportunity.
You will be responsible for preparing, analyzing, and interpreting operational revenue results using internal and external data sources.
Responsibilities:
Prepare and analyze monthly, quarterly, semi-annual, and annual brand level variance analysis for sales revenue & volume and cost of sales
Develop and maintain KPI / Scorecard of vital business statistics for sales brand lines as a monthly financial review and provide key drivers to variances
Provide detailed analysis on Price, Volume and Mix of the Portfolio by brand
Develop / Network relationship with Commercial Organization to gain regional insights explaining sale variances to Forecast, Budget and Prior Year by brand
Risk / Benefit analysis on forecast and budget variances to ensure management understands the financial impact
Consolidations and presentation of prepared analyses
Identify trends in financial performance and providing analytics commentary
Provide analytical support to functional initiatives, such as participation in new product launches to analyze market share, pricing, share of wallet and regional competitor comparative
Provide ad hoc reporting and modeling support to multiple cross-functional team members as needed
Assist in preparing and implementing new financial systems, tools and methods


Background / Qualifications
Bachelor or Master’s in Finance, Accounting, Math, Statistics, and/or Business Analytics
Prior FP&A experience or 5+ years of progressive related experience a plus
Ability to communicate and make presentations to Senior and Executive Management
Skilled at analyzing large volumes of data with an ability to synthesize into trends and actionable recommendations
Advanced modeling, reporting, and forecasting skills with proven mastery of Excel
Strong analytical, problem-solving skills and business acumen
Ability to successfully operate within a remote or geographically decentralized environment
Ability to mindfully communicate both verbally and in writing
Possesses intellectual curiosity, and a passion for detail, accuracy, and completeness
Experience with Power BI, Hyperion, Anaplan, Oracle, Essbase, and/or SASS databases a plus


Preferably we want to fill this position as soon as possible and will assess candidate on a continuous basis, however finding the right individual is our top priority.
We look forward to hearing from You. Visa mindre

Söker du utveckling inom drift och underhåll med möjlighet att utmana och utveckla våra högautomatiserade maskinanläggningar i Mölndal?
Vi kommer under året starta ytterligare högautomatiserade maskinanläggningar i vår produktion i Mölndal och vi behöver därför utöka vår grupp med ytterligare en Maintenance and Operating Technicain.
Om rollen. I rollen kommer du att arbeta med underhåll inom vår produktionsanläggning som innefattar monterings-, bearbetnings- och förpackningsmaskiner samt en renings- och processanläggning där du kommer vara maskinansvarig för en maskin eller område.
Dina huvudsakliga arbetsuppgifter är;
driva förbättringsarbete på ditt område tillsammans med tvärfunktionell grupp som arbetar med utveckling av produkt och maskinområde
utveckling, testning, förbättring och driftsättning av nya och befintliga maskiner/processer tillsammans med andra avdelningar
driva arbete med att utveckla och förvalta förebyggande och avhjälpande underhåll för att bibehålla och säkerställa stabila processer på våra produktionsutrustningar


Vem är du Vi ser att du är drivande och engagerad som person och vill vara med att förvalta och utveckla processer i en högautomatiserad produktionsmiljö tillsammans med dina kollegor i teamet
Vi ser att du har
dokumenterad teknisk kompetens och erfarenhet inom drift och underhåll
ett utmärkande kvalitets- och ett högt säkerhetstänkande
en kostnadsmedvetenhet med fokus på effektivt och långsiktigt underhåll
en hög kommunikativ förmåga, eftersom rollen innebär att du ska kunna kommunicera förtroendefullt, pedagogiskt och tydligt med personer på flera olika nivåer som har olika teknisk kunskap


Bra att veta För mer information, ring gärna rekryterande chef, Markus Kristiansson, telefonnummer +46 31 376 33 26.
Ansökningar kommer att hanteras löpande, så skicka in din ansökan snarast möjligt.
Om Wellspect HealthCare Wellspect HealthCare, med huvudkontor i Mölndal i Sverige, är en ledande global leverantör av innovativa medicintekniska produkter och tjänster med fokus på hjälpa människor som lider av urinretention eller kronisk förstoppning. Varje dag arbetar mer än 1 100 engagerade medarbetare med att göra skillnad för de som behöver våra produkter och våra tjänster. Många av dem som vi hjälper har ryggmärgsskada, förstorad prostata, ryggmärgsbråck eller multipel skleros. Vi är en av världens ledande tillverkare av intermittenta urinkatetrar, med LoFric® som vårt mest kända varumärke. Som hjälp till de med kronisk eller svår förstoppning har vi utvecklat vad som sannolikt är världens mest avancerade irrigationssystem, Navina Systems™, vilket kombinerar en hög grad av användarvänlighet, klinisk effekt och kommunikation i ett verkligt smart system. Wellspect HealthCare är representerat i fler än 30 länder samt ingår i Dentsply Sirona, världens största tillverkare av professionella tandvårdsprodukter och teknologier med huvudkontor i North Carolina, USA. Företagets aktier är listade på amerikanska NASDAQ under symbolen XRAY. Mer information finns på www.wellspect.com och www.denstplysirona.com. Visa mindre

Challenge yourself and explore new ways to make a real difference by joining our QC-team.
About the position As a Quality technician you will be a part of a team of committed members focused to ensure Wellspects world class quality. Our continuous goal is to broaden and deepen every members’ unique competence and by that improve our role as Quality Control.
Your key accountabilities consists of;
Incoming inspection of components
Final inspection of ready-made products
Review of batch records
Measuring tasks for various quality assurance activities
Quality development activities in cross-functional teams

Who you are: You are proactive, creative and analytical. You have good skills in reading and understanding instructions and specifications. You have basic knowledge of common statistical tools and analyzes. You also work with a high degree of integrity and dare to question the answers.
We believe you have:
a college or equivalent background
experience from regulated business
a careful, responsible and structured way of working
good writing skills as we have high demands on documentation
good communication and interpersonal skills as parts of the work is done in cross functional teams
full command of both Swedish and English language
good knowledge of standard Microsoft Office applications
basic knowledge of standard statistical methods

It is considered an advantage if you have experience from Statistical Process Control and/or if you are familiar with regulations for medical device (i.e. ISO 13485, MDD 93/42/EEC, FDA QSR)
Good to know For more information, contact recruiting manager, Bertil Langervik, telephone +46 31 376 34 55.
Please note that we will review applications continuously, so be sure to send in your application as soon as possible. Visa mindre

Do you want to work in a global organization and be part of creating innovative solutions for healthy smiles? Have a look at the description below. Maybe it’s you we are looking for.
As a Quality Engineer, your focus will be on the Products and Design Control. Represent QA in Product Development Project and work in cross-functional teams in a global environment. Participate in Design Reviews and actively be part of development and establishment of a robust process with appropriate Quality Control Measures. Be responsible for Measuring Machines and develop future measurement methods with suppliers.
Responsibilities:
team member in Product Development Projects with focus on Design Control
develop and implement validated method for Quality Control
support and perform measurement assignments
act as Instrument Owner for Measurement Machines in the QA Lab
develop measurement methods with suppliers
lead and participate in Improvements Project related to Quality



You are a flexible and positive team player. Enjoy problem solving and have analytical skills. You are open for challenges and enjoy working together with highly skilled and dedicated colleagues where every day makes a difference.
Qualifications / Background
Master or Bachelor degree in engineering, science or technical discipline
preferably 3 years of experience within Quality Assurance
experience from measuring machines and instruments
experience from working in Global cross-functional Projects
a strong commitment to achieve goals and targets
analytic and structured approach of working
good communication in English as well as Swedish, both written and verbally
interpersonal skills as parts of the work is done in cross functional teams
it is considered an advantage if you are familiar with ISO 13485, ISO 14971, MDD 93/42/, MDR 2017/745 and FDA Quality System Regulation or have experience from product areas with high regulatory demands


Dentsply Sirona can offer you an exciting and challenging job in a global company that is committed to make a difference every day. We are a diverse and dynamic team that believe in continuous development. We have a team spirit culture where sharing knowledge and jointly finding new ways to tackle challenges is key.
This position is located in Mölndal, Sweden.
For more information, please contact recruiting manager, Micael Andersson, telephone +46 31 376 34 88.
Apply no later than 19th of September 2021. Please note that we will review applications continuously, so be sure to send in your application as soon as possible. Visa mindre

Join our Production Development team and continue shaping medical device production systems of tomorrow.
As a Production Engineer with a focus on Automation and Production systems, you will play a key role in the development and implementation of New and improved production processes at Wellspect. In this role you will interact with various stakeholders, from understanding the product configuration to developing system requirements and issue technical specifications for an efficient production flow. In the role you will also be accountable in the design of the final automated solution and its implementation to the actual production processes. We are proud to have an in-house, highly automated medical device production with interconnected coating processes, multiple transport systems and packaging machines. And as a leading medical device manufacturer we have strict requirements on material traceability and in-line quality control. Applying Big Data principles and develop machine learning in an Industry 4.0 spirit is also a vital part in the design and development.
Responsibilities:
Industrial IT/automation project management in cross-functional development projects in various stages from concept to commissioning and handover.
Design, risk and requirements handling as well as testing and validation of control systems for highly automated production of Medical Device products.
Develop documentation in compliance with our quality management system built on regulatory requirements from the European medical device directive and FDA quality systems regulations.
Integration of machine line and components with a systems perspective on process control, traceability and communication with MES/SCADA and PDM systems.
Contribute in Wellspect’s digitization development strategy e.g. collection of data for analysis and application development
Establish and maintain good working relationships with our internal suppliers and stakeholders as well as our external supplier also including evaluations and supplier visits.


We think you are a positive, systematic and driven team player. You are open for challenges and enjoy working together with highly skilled and committed colleagues.
Background / Qualifications:
an academic background, preferably in automation, electrical/computer engineering or equivalent
experience in production development with focus on control systems in automated production
an in-depth understanding of industry control systems and experience in programing
experience from working with developing technical specifications and working with external suppliers
technical project management experience
experience from testing/validation, preferably within life science or other highly regulated industry
knowledge of databases, and PLC/HMI/SCADA, preferably Siemens Simatic products.
knowledge of ISA 95 and ISA 88 standards are considered a plus
documentation and communication skills, in English as well as in Swedish


Wellspects’ production is in continuous evolvement and there are always new and interesting projects going on. We offer you a place to develop your skills as part of a cross-functional team and the medical devices we manufacture make a real difference in the lives of our users. That’s a reason to go to work!
For more information, please contact recruiting manager, Anders Fagerström, telephone +46 31 376 33 73.

Please apply no later than August 22nd , 2021. Please note that we will review applications continuously, so be sure to send in your application as soon as possible. Visa mindre

Join our team as we are expanding into new fields where embedded systems will play a vital role.
As R&D Engineer – Systems Design at Wellspect you will work in our Research & Development department and have a key role among mechanics, hardware and software developers, internal projects and suppliers. You will be part of a cross functional team that take us forward in the area of embedded systems in the medical device area.
Your focus will be to bring in new technology to the company, perform concept studies in pre-development projects and to create the system architecture for the complete medical device system in product development projects. The systems involve embedded sub systems, application SW, mechanical subsystems and single use components.
You will contribute to build up the new core competence by sharing your knowledge and experience in systems engineering to the rest of the team and defining the way of working, i.e. processes and tools.
Responsibilities;
Be involved in technical requirements and risk management activities.
Transform user needs, market requirements and regulatory requirements into a solid system design and more detailed technical specifications.
Technical lead.
Be a point of contact with internal R&D, external development partners, production, suppliers and a number of stakeholders in the development- and life cycle management process.



Join our team where we challenge and explore new ways in our effort to continuously improve ourselves, individually and as a team. This is a great opportunity if you want to work in a successful company with products that makes a real difference.
We believe you are a positive team player with a holistic view. You enjoy solving technical problems, thrive in a challenging environment and enjoy working together with highly skilled and committed colleagues.
Qualifications / Background:
An academic education (M.Sc or B.Sc.) in electronics/mechatronics, software or similar.
At least 5 years documented experience in systems engineering for advanced products covering Mechanical parts, HW and SW.
At least 5 years documented experience in electronics or mechatronics detailed design.
Very high understanding in mechanics and material.
Used to work with standards.
Used to write technical documentation (specifications, design plans, reports, analysis etc)
It is highly meritorious with experience in developing advanced products within medical.device, functional safety or any other field involving personal safety aspects.
Strong drive to achieve goals and targets.
A creative mindset with strong analytical skills.
Great communication skills in English and Swedish, both written and verbal.


For more information, please contact Stefan Miholic, phone +46 31 3764267.
Please apply no later than August 30th, 2021. Visa mindre

Do you want to improve peoples’ lives with medical devices that make a real difference? Now you have the opportunity as Wellspect HealthCare is looking for a new Market Labeling and Product Manager.
The Market Labeling and Product Manager role combines the responsibility to ensure that our medical devices are labeled with the right information and a responsibility for one of the latest additions to Wellspect’s product portfolio.
As responsible for labeling of products within the Enterology platform, you will lead and coordinate the introduction of new and changed information affecting the labeling and Instructions for use. This role requires a structured hands-on approach for ensuring the information and symbols are according to regulations and understandable to users and healthcare professionals. You will also be involved in new product development projects and play an active role when entering new markets.
In the other part of the role you will have strategic responsibility for a range of products within Wellspect’s Enterology portfolio during their entire life cycle including product positioning and marketing activities. With your excellent skills as well as your ability to analyze market trends you will develop and execute strategies to support sales growth together with colleagues around the globe. You will gain clinical and business understanding of user needs; co-operate with an external partner and be the go-to person for product related questions.
Both aspects of this role require active collaboration with all company functions, our commercial entities around the world as well as other external stakeholders such as advertising agencies and translation providers.
Responsibilities:
Plan, lead and prioritize activities to develop new or change the product labeling including instructions for use while closely collaborating cross-functionally with relevant stake holders.
Coordination between HQ and our commercial entities around the world regarding product and labeling changes and understand the market and business effects of such changes.
As the key stakeholder and labeling responsible, you will participate in product development projects to ensure compliance with relevant regulations and understandable instructions.
Manage all aspects of the product(s) life cycle starting with understanding of the market needs until the product is phased out. This includes prizing, marketing, supply chain related topics, labeling, registration, clinical evidence as well as legal and safety requirements to ensure sustainable profitability, growth and market share.
Set direction and support the creation of product, education and communication material together with the Marketing Communication Manager.
Stay up to date on industry trends and competitor products and activities.



We think you are an organized problem solver, a team player and an efficient communicator. You take pride in your solutions and in getting things done. You are open to challenges and enjoy working with many different contacts. Experience from an international environment will be regarded as an advantage. You are inspired by our values and a sense of good humor comes naturally to you.
Background / Qualifications:
An academic background (M.Sc./B.Sc.) in Product Management, Business economics, Marketing, Life Sciences or similar.
Business oriented mindset and project coordination skills.
A structured way of working; taking pride in getting things right.
An understanding of medical device labeling standards and experience working with instructions and external suppliers will be considered an advantage.
Some experience in product management, marketing and/or sales preferably within the Medtech/Life Science industry/Food industry or similar.
Strong communication skills and an ability to build lasting relationships both internally and externally.
Full command of the English language, both written and spoken and preferably a good understanding of Swedish.
Knowledge and experience with InDesign software, Product data and/or change management software is considered an advantage.



We can offer you an exciting and challenging job in a company that is committed to make a difference every day. We have a culture of team spirit, where sharing knowledge and finding new ways to tackle challenges together is the key.
This position is based at our headquarter in Mölndal, Sweden and will involve occasional travelling to build and maintain relations. For more information, please contact recruiting manager Thomas Börstell (available from Aug 16), phone +46 31 376 43 25
Please apply no later than Aug 22th 2021. We will review applications continuously. Visa mindre

Join our team where we bring out the best in people in our effort to make a difference.
In our team we work together to improve our processes and become even more automated and efficient. Collaboration is essential and we hear that employees describe our atmosphere as open and welcoming. We have a lot of interesting projects ahead of us and this is where you can make a difference bringing in your technical expertise. You will be part of a team with highly skilled colleagues and we can promise you both challenges and fun at work. If this is this something that you value, then this might be the opportunity for you.
The Production Technology departments’ responsibilities are improvements of existing manufacturing processes, industrialization of new products as well as procurement and validation of new production process equipment for implant production.
Responsibilities:
Leading and developing your team of Production Engineers, Mechanical Designer and Production Documentation Coordinators responsible for:
process and machine improvements projects in production, both locally and globally
introduction of product changes and the handling of process deviations
investment projects of new machinery/ equipment in accordance with current regulations
Drive and coach your team toward set goals to deliver production development projects on time, within budget and with desired performance.
Guide and coach your team on the implementation of Lean Production and Design for Manufacturing principles in equipment
Participate in cross-functional teams to find efficient ways of working with product and production development.


We think you are a positive, driven team player and efficient communicator. You are open to challenges and enjoy working together with highly skilled and committed colleagues where every day makes a difference.
Background / Qualifications:
an academic background, preferably in Mechanical/Automation Engineering or equivalent with experience from production development.
More than 3 years of management experience with personnel responsibility and experience of project management
proven leadership skills in leading teams and experience in driving change processes within the organization.
Ability to coach your employees to achieve our common goals.
knowledge of automated manufacturing process development and working with external equipment suppliers.
some experience from testing/validation, preferably within life science or other regulated industry.
documentation and communication skills, in English as well as in Swedish.


For more information, please contact recruiting manager, Jan Andersson (Head of Production Engineering) at +46 31 3763200.
We will evaluate application on a continuous basis so don´t hesitate to send us your CV.
Welcome with your application. Visa mindre

Are You experienced in Clinical Research? Would you describe yourself as a hands-on type of person with a natural talent for solving issues and pushing for progress? Then we may have the right position for you! Reporting to the Head of Global Medical Affairs, you will be part of an agile team of clinical research experts developing clinical evidence to support commercial needs and regulatory requirements.
As Global Clinical Project Manager at Wellspect you are driving prioritized clinical projects. Adherence to quality, timelines and budget comes natural for you. The role requires a scientific mindset and ability to get things done. To succeed in this role you are dependent on successful collaborations with internal and external stakeholders.
Responsibilities:
Accountability for all parts of clinical project execution, ie from protocol development to report finalization
Compliance with applicable standards, rules and regulations
Ability to drive a variety of project types (e.g. size, design, geographies, indications, phases)
To manage dynamic and multidisciplinary study teams including external vendors
To represent the function in cross functional forums, eg. development projects and during audits


Qualifications / Background
Relevant medical/scientific degree, typically on MSc level
3-5 years of relevant and documented experience, preferably within Medical Device
Good knowledge in applicable regulations and standards governing clinical research eg. ISO 14155/GCP and MDR
Insight in medical device development and life cycle requirements is an advantage
Statistical and data management knowledge is beneficial, as is vendor management experience
Proficient in English (verbal and writing)


We believe that you are a positive, solution-oriented and hands-on type of person with a strong sense of accountability for your work. You enjoy the mix of working in a team as well as independently, always with an appropriate sense of urgency. You challenge and explore status quo with a clear ambition to add value, constantly striving for efficiency improvements.
The position includes some travelling. Preferably we want to fill this position as soon as possible and will assess candidate on a continuous basis, however finding the right individual is our top priority.
We look forward to hearing from You. Visa mindre

Vi söker en Ekonom inom Kundreskontra till vår Ekonomiavdelning i Mölndal. En fantastisk möjlighet för dig som vill jobba i en internationell miljö med produkter som gör skillnad!
Du kommer som Ekonom att jobba i en grupp med högpresterande Controllers och Accountants. Tillsammans har ni ansvar för flera legala enheter inom Norden och rapporterar till chef i Mölndal. I teamet jobbar ca 20 personer.
Ansvarsområden:
· Hantering av kundreskontra
· Påminnelsehantering
· Kontaktperson vid inkasso
· Släppa spärrade kundordrar
· Koncerninterna betalningar
· Koncerninterna avstämningar för kundreskontra/levreskontra
· Manuella betalningar
· Kontoavstämningar
· Ekonomirelaterade projekt

Kvalifikationer/Bakgrund:
· Kandidatexamen eller motsvarande akademisk bakgrund inom Ekonomi
· Minst tre till fem års erfarenhet inom ekonomi
· Erfarenhet från något av de vanliga affärssystemen, meriterande är erfarenhet av Movex
· Goda kunskap i Microsoft Office
· Erfarenhet från projektarbete är meriterande
· Tala och skriva svenska och engelska obehindrat
Vi tror att du är en lagspelare som är analytisk och problemlösare. Du har en hög grad av noggrannhet och öga för detaljer samt är en god kommunikatör. Du gillar utmaningar och förändringar samt att arbeta i en internationell miljö med motiverande arbetskollegor.
Denna position är placerad i Mölndal.
För mer info kontakta rekryterande chef Anders Magnusson, +46 31 376 31 43.
Ansökningar hanteras löpande, så se till att skicka in din ansökan så snart som möjligt.
Välkommen med din ansökan! Visa mindre

Do you want to work in a company where you can make a real difference, where you have room for creativity and your expertise counts? In this role you will combine science and evidence development with understanding of commercial opportunities. Does this sound exciting?
The role resides with Global Medical Affairs, part of Global Marketing at our headquarter in Mölndal, Sweden. You will be responsible for the central management of health economics across therapy areas and products. Thorough understanding of the business, strategies and priorities is key. Your contribution as subject matter expert covers new product development projects as well as support to the business and marketed products. You will have stakeholders and close collaborators across the organization, including subsidiaries.
Responsibilities
To initiate and manage health economic projects of various types.
To analyze external data and scientific literature.
Reimbursement know-how and oversight.
Development of material to demonstrate and communicate the value of products, solutions and therapies.
To manage a relevant network of internal and external stakeholders.
Contribute with market intelligence as required by commercial priorities.
The work may include project managing external resources.

Qualifications / Background
Relevant academic degree within Health Economics, preferably MSc or above.
A background in similar roles, e.g. Health Economics Outcomes Research (HEOR), within Medical Device is an advantage.
You have documented experience in how to optimize health economic evidence to support local and global business initiatives.
You have a proven commercial acumen.
Statistical knowledge and Market intelligence experience are considered a plus.
You are proficient in English (verbal and writing).
Swedish speaking is an advantage but not a prerequisite.


The preferred candidate has the drive, endurance and capability to set, and execute on own goals and KPIs. You have a hands-on approach and comfortably acts in cross functional teams as well as independently. You take initiatives, are creative and rise with a challenge. You have a positive attitude and you are a strong communicator who is perceived as highly professional by peers and stakeholders.

We will evaluate applications continuously so don´t hesitate to send us your application. We look forward hearing from you. Visa mindre

Join us in a key finance role leading the team to provide service that create value. We have an exciting journey ahead of us and can promise you both success and challenges. With us you will have an international environment that offers possibilities for growth. Are you the leader we are looking for with a thorough knowledge from transaction and accounting then don´t miss this opportunity.
Responsibilities
As Manager for the Accounting Transaction Services team, you will hold an important role within the Nordic region and manage a team of 12 persons. The Transaction Services department has overall responsibility for accounting transactions for 7 legal entities. The department’s main responsibilities are Accounts Receivables, Accounts Payables, General Ledger, Fixed Assets, Travel Expenses and Projects. The company is in a process of transformation and you will play an important role in the transformation work for the Nordic region. You will lead the work with Intelligent Automation and drive the Robotic Process Automation (RPA) implementation for Finance. You will ensure quality and compliance with existing processes, as well as initiate and implement system and process improvements.
Background / Qualifications
Bachelor’s or Master´s degree within accounting.
A minimum of 5 – 7 years working experience from accounting and transactions.
Preferably a few years’ experience from leading teams.
A great interest in IT.
Previous experience of managing projects and seeking improvements within the field.
Fluent in both written and spoken English as well as Swedish.
Preferably you are familiar with Movex.
Desirable Robotic Process Automation knowledge.


We work in a changing environment and it is essential that you are flexible, positive and have a down-to-earth approach. You focus on the team as opposed to individual performance. You are a natural leader with excellent communication skills and providing service is vital to you.
For more information, please contact recruiting manager, Anders Magnusson telephone +46 31 376 31 43.
Please apply no later than June 30, 2021. Please note that we will review applications continuously, so be sure to send in your application as soon as possible. Visa mindre

We are hiring an Accounts Receivables Accountant to join our Finance team in Mölndal, Sweden. A great opportunity if you want to work in an international environment with products that makes a difference.
As Account Receivables Accountant, you will work in a highly motivated team with responsibilities for several legal entities across the Nordic region.
Responsibilities:
Account Receivables
Customer Payments processing
Reminders
Contact person Collection
Order Release
Netting Payments
IC reconciliation AR/AP
Manual payments
Account Reconciliations


Qualifications / Background:
Bachelor’s degree (B.A.) or equivalent academic background in Finance
Minimum three to five years of experience
Experience in one of the commonly use accounting ERP systems, preferable Movex
Proficiency with Microsoft Office



We think you are a team player with analytical and problem-solving skills. High degree of accuracy and attention to details with excellent communication skills. You are open for challenges and enjoy working together in an international environment with highly skilled and committed colleagues.
This position will be located in Mölndal, Sweden.
For more information, please contact recruiting manager, Anders Magnusson, +46 31 376 31 43. Please note that we will review applications continuously, so be sure to send in your application as soon as possible.
Welcome with your application! Visa mindre

Join our Production Development team and continue shaping our medical device production of tomorrow.
The Production Development departments are responsible for improvements of existing manufacturing processes and industrialization of new products as well as procurement and validation of new production process equipment for medical device production. At Wellspect, we are we proud to have a highly automated in-house production with chemical processes, multiple transport systems, assembly and packaging lines producing medical devices in large volumes 24/7.
Responsibilities:
Leading and developing your team of Production and Validation Engineers responsible for development, installation, commissioning and validation of new and improved production methods and processes.
Drive and coach your team towards set goals to deliver production development projects on time, budget and with desired performance.
Guiding and coaching your team on the implementation of Lean Product Development and Design for Manufacturing principles in equipment investment projects with focus of Automation System Design, Digitalization within production and Validation of production processes.
Member of the Production Development Management team.
Participate in cross-functional teams to find efficient ways of working with product and production development.
Ensuring resource allocation and utilization of team and consultant linked to Wellspect’s business needs


We think you are a positive, driven team player and efficient communicator. You are open for challenges and enjoy working together with highly skilled and committed colleagues where every day makes a difference.
Qualification / Background:
an academic background, preferably in Mechanical/Automation/Industrial Design Engineering or equivalent with experience from production development.
many years of management experience with personnel responsibility and experience of project management, especially within new product development and industrialization.
proven leadership skills in leading teams and experience in driving change processes within the organization.
communicative ability and the ability to coach your employees to achieve our common goals.
knowledge of automated manufacturing process development and working with external equipment suppliers.
knowledge of Digitalization within production, Automation System Design and Risk Management.
some experience from testing/validation and quality management processes, preferably within life science or other regulated industry.
documentation and communication skills, in English as well as in Swedish.


For more information, please contact recruiting manager, Anders Westling, telephone +46 31 376 42 70.
Please note that we will review applications continuously, so be sure to send in your application as soon as possible.
Welcome with your application! Visa mindre

Are You good at, and enjoy, writing clinical documentation and building clinical strategies?
Then maybe you are ready for a key role at one of the leading global providers of medical devices within bladder and bowel continence care?
You will be a member of the Global Medical Affairs department, we are an agile group of experts waiting for You to join us in the important work of planning, generating, evaluating and documenting scientific evidence to meet commercial needs and regulatory requirements. If this sounds interesting, please keep reading.
As specialist in putting clinical evidence into a business and regulatory context the role requires high scientific knowledge, medical writing capabilities, integrity and a broad understanding of external requirements/internal strategies. You will be one of two colleagues managing clinical evaluations and driving the cross functional evidence planning for Wellspects full range of products.
Responsibilities:
Management of all deliverables related to Clinical Evaluations
The development of Clinical Evidence Programs i.e. to lead cross functional planning forums to support business objectives
To define, and follow up on, Post Market Clinical Follow-Up initiatives including managing PMCF-surveys
To optimize the use of clinical evidence to support successful registration, positioning and life cycle management
To represent the function in external (e.g. audits, inspections) and internal (e.g. projects and meetings) forums as subject matter expert
To contribute from early product development and throughout the products life cycle

Qualification / Background:
PhD degree, or equivalent
Approximately 5 years of documented relevant experience, preferably in conducting Clinical Evaluations
Documented experience in clinical research planning e.g. study designs/methodologies
Documented experience in scientific writing, literature search strategies and analysis
Thorough understanding of applicable regulations and guidelines such as MDR and MEDDEV 2.7.1.
Understanding of medical device development and product life cycle requirements
Clinical experience, preferably within Urology a/o Enterology, is an advantage
Proficient in English (verbal and writing)


We believe that you are a positive and driven person with the ability to extract, and communicate, relevant information from various sources such as scientific publications, reports and post market surveillance data. You are excellent in writing regulatory documentation. You strive for progress and are comfortable in managing cross functional forums. You are used to work independently digging deep into extensive data sources, yet with an appropriate sense of urgency. Strong stakeholder management is key as your success partly is based on your cross functional interactions. You challenge and explore status quo with a clear ambition of constantly improving our way of working.
We are interviewing candidates continuously, so to enhance your chances, we recommend that you send us your application as soon as possible.
We look forward to hearing from You. Visa mindre

If you live and breathe digital marketing, we want to talk to you. We are looking for a Digital Marketing Manager to develop, implement, track and optimize our digital marketing campaigns across all digital channels and markets.
You will play a key role taking Digital Marketing to the next level and being able to influence our way forward. In this role you can really make a difference and we can promise you an exciting journey.
You should have a strong grasp of current marketing tools and strategies and be able to lead integrated digital marketing campaigns from concept to execution. Our new Digital marketing manager will join a team of digital marketing specialists and work with the Central marketing team, local marketing teams and agencies.
Responsibilities:
Plan and execute digital marketing, including SEO, email, social media and digital advertising campaigns
Measure and report performance of digital marketing campaigns
Utilize strong analytical ability to evaluate end-to-end customer experience across multiple channels and customer touch points
Collaborate with internal teams to create landing pages and optimize user experience
Collaborate with agencies and other vendor partners
Evaluate emerging technologies, identify trends and provide thought leadership and perspective to optimize spend and performance
Identify and implement on-line monitoring tools

Background / Qualifications:
Degree in marketing or a related field and/or proven working experience from digital marketing
Strong analytical skills and data-driven thinking
Up-to-date with the latest trends and best practices in online marketing and measurement
Experience in creating relevant user journeys
Solid knowledge of inbound marketing tools (e.g. Pardot, Hubspot, Marketing cloud), website analytics tools (e.g. Google Analytics), CRM and CMS platforms
Experience in optimizing content for SEO performance


Preferred location is our Headquarter in Mölndal / Gothenburg, but we are also open to someone who can work remotely from any of our larger sites in Europe. You will report into our Head of Corporate Marketing Communication.
Please note that we will review applications continuously, so be sure to send in your CV as soon as possible.
We look forward to receiving your application! Visa mindre

Are you interested in joining an agile team of experts linking medical information to regulatory requirements and ultimately commercial interests within the Dental Implants business? We see this role being strategically important as we can make a difference when it comes to getting our products out on the market.
We are currently looking for a Regulatory Compliance Manager to strengthen our organization. You will work in an international environment with enthusiastic people and continuously develop our business to meet new demanding requirements.
Responsibilities:
• Develop strategies and plans for registration of new or changed products in close cooperation with the registration holders at the Commonwealth of Independent States (CIS).
• Compile registration documentation and manage registration of new / changed products according to the company strategies and plans.
• Review device labeling, labels and advertising material for compliance with regulatory requirements and applicable laws.
• Perform classification of products.
• Maintain current knowledge of Rosdravnadzor registration procedures and the new Eurasian Medical Device Registration Rules (ERR)
Qualifications / Background:
• A MSc in engineering or natural science or an equivalent professional background.
• Experience from writing regulatory applications for medical devices products for entering the CIS market.
• Experience from working in a medical device industry and have knowledge about ISO 13485
• Strong communication skills in English and Russian, both written and spoken.
As Regulatory Compliance Manager in a global business environment, we believe you have analytical skills and enjoy creating creative solutions. You want to be part of shaping an industry and enjoy working together with highly skilled and committed colleagues where every day makes a difference.
The position will primarily be in Mölndal, Sweden but other DS sites could be discussed. The position will report to the Director of Regulatory Compliance. For more information, please contact recruiting manager, Lena Lindblad, telephone +46 72 52 55 751.
Please note that we will review applications continuously, so be sure to send in your CV as soon as possible.
Welcome with your application! Visa mindre

We are looking for a Senior Clinical Advisor to join our team and be part of our journey to continue drive innovations. This is a key role where you will be able to influence the way forward and meet with the Key Opinion Leaders and other experts in the area of dental implants.
As market leaders we shape the industry and we have a passion for innovation. In this role you will be the voice of the customers and be on top of the latest science within your expertise.
Don´t miss this great opportunity!

Responsibilities
Provide clinical and technical leadership, support, and supervision during new product development and product maintenance
As Clinical Officer take part in assigned tasks and activities according to processes and routines
Provide technical support towards development of concepts and cross product portfolio solution services
Assist in the assessment of clinical training needs and in the design and implementation of appropriate measures to address those needs
Liaise with the relevant functions to develop high impact product and service offerings
Act as Clinical Affairs representative in projects or support projects in areas related to technical and clinical expertise
Identify and disseminate best practices, market trends and new technical strategies and approaches in areas of expertise
Review clinical assets for training and marketing materials
Oversee development of product promotion material that needs clinical and technical knowledge
Support in clinical assessment for concessions, risk assessment etc.
Participate in training activities internal as well as external


Qualifications / Background
Education:
Doctor of Dental Surgery (DDS)
Post graduate education as specialist in Prosthetics, Perio or Surgery; Oral Surgeon on Maxillo Facial Surgeon

Experience:
Minimum 5 years practice as specialist working with dental implants
Extensive experience from dental implant practice.
Experience in case documentation and photography are welcome
Experience as lecturer/author of CE articles welcome


You will be part of a highly skilled and committed team. In this role it is important that you are open for input from others at the same time as you need to have the confidence to stand up for your expertise. Excellent communication skills will be essential and the ability to influence people around you. You will work with many different contact settings and teamwork will be an important factor for success.

Please note that we will review applications continuously, so be sure to send in your application as soon as possible. For more information about the role please contact Björn Delin Vice President Global Clinical and Scientific Support at +46 705 767260.

We look forward hearing from you! Visa mindre

Do you want to be part of a company where everything you do make a difference? As a world leading dental company with the ambition to continue to drive innovations for the dental professionals, we can promise you an exciting and challenging environment.
We are now looking for a Strategic Buyer to join our EMEA team. In this role you will have the opportunity to influence on our way forward and being part of setting our structure. You will be part of a global team where we support each other and work together to reach our goals.
We are looking for someone to support multiple Indirect categories/projects. You will work towards different regions and will work cross functionally with many different contact settings. In this role you will partners with regional and global category management to ensure a successful implementation of global or regional led strategies and drive compliance to preferred supply base and purchasing channels. The role is responsible to ensure and continuously improve costs, quality and service level / delivery for all local deliverables in multiple categories.

Responsibilities:
Support the implementation of global and regional category strategies.
Support regional/global RFPs.
To partner with relevant stakeholders.
To cooperate and support internal stakeholders at projects.
To execute design to cost opportunities across all sites, ensuring working capital efficiency.
Guide and support the tactical buying for Indirect Materials & Services.
Ensure that Indirect materials and services are delivered in-time.
Collaborate with COE team to implement the Procurement processes & compliance requirements across the sites.
Supplier Relationship Management.
To perform negotiations with suppliers and sign contracts.
To support annual procurement targets for the site in alignment with global/regional targets (cost & savings, supplier quality, etc.).
Support Regional Sourcing Leaders with regular updates to ensure effective communication of cost saving activities.
Proactively identify saving potentials.



Qualifications / Background
Bachelor’s degree or equivalent in a related discipline.
A minimum of 2-3 years professional experience in purchasing of Indirect material.
Strong relationship building and leading by influence skills.
Experience from identify and lead cost improvement initiatives will be a merit.
Strong business partnering skills and business acumen.
Assertiveness and ambition to solve demanding tasks.
English fluent in written and spoken. Other languages welcomed.



We are looking for someone with a multicultural and proactive mindset who has strong analytical skills. You are result oriented, flexible and able to adapt to changes. For this role you need strong communication and networking skills with the ability to influence others.
Do you get energy from working in an environment with a high pace and challenging tasks then don´t hesitate to contact us.
Please submit your application in English, no later than May 2nd, 2021.
We will review applications continuously, so be sure to send in your application as soon as possible.
Welcome with your application! Visa mindre

A great opportunity for you who wants to work as Project Manager with products that make a real difference.
As Project Manager at Wellspect Healthcare, you will be the tactical and operational team leader with complete ownership of project results, agile pacing, resource balancing and financial control of the projects within Wellspects New Product Introduction portfolio. You will plan, organize, lead and control projects to ensure on-time and qualitative delivery within the projects. Our recently launched strategy will also enable opportunities for you to potentially lead change and improvement projects.


You will become part of a team where we challenge and explore new ways of working, in our effort to continuously improve ourselves, individually and as a team. Our team culture is described open and supportive, together we are moving our portfolio to the next stage. This is a great opportunity if you want to work in a successful company with products that makes a real difference.
Responsibilities
Leading projects in compliance with corporate policies, quality and management systems within Wellspect, existing laws and regulations as well as standards and agreements.
Planning, organizing, directing and controlling projects according to company development process
Lead development projects for new products and upcoming generations
Continuously improve our project working procedures according to Lean Product Development principles


We think you are a positive team player with holistic view that enjoy creating result. You are open for challenges and enjoy working together with highly skilled and committed colleagues. To be successful in this role you are motivated by developing and driving projects forward and enjoy reaching goals as a team. Planning and organizing is something that comes naturally to you and you thrive in a coaching/leading position.
Qualifications / Background
an academic background
extensive experience from working with product development in a project leading position
you can also have a background as management consultant
it’s an advantage if you have experience from working as a line manager in a technical product environment or complex environment


As documentation is a big part of the job, excellent communication skills in English and Swedish, both oral and written are essential.
This position is located at our headquarter in Mölndal, Sweden
For more information, please contact Anders Tennby, recruiting manager and Head of Project Portfolio Management, phone 031-376 44 02.
Please apply no later than April 21, 2021. Please note that we will review applications continuously. Visa mindre

Do you want to work within science and clinical studies in a global environment? What we do really make a difference to people’s lives. We give people their smiles back, and I can promise you it is rewarding being part of what we do. In this role you will be a key player making sure our products reaching the market are safe and compliant.
Come and join our engaged Clinical Research team!
Global Clinical Research at Dentsply Sirona Implants are responsible for the planning and performance of clinical studies. This can be sponsored studies on non-approved products as well as on regulatory approved and marketed products, where you will work in a global setting. In this role you will prepare the required study documents, including time plans and study agreements. You will work in close collaboration with other departments, as well as with dental clinics and universities worldwide.
Responsibilities
Plan and execute clinical studies:
Preparation of study documents
Monitoring at site, data management and follow up on study budget
Analyze, report and present study results at investigators meetings
You will also be the Clinical Research representative in relevant Product development projects


Qualifications / Background
Higher education in natural science
Background in dentistry and/or research
Experience working within Medical device
Knowledge of the regulations for human clinical trials
Fluent English in writing and speaking


As a person you have a scientific view and you are market oriented. You will need to be structured and creative with a drive for result. Good collaboration skills are essential as well as strong communication.
The position will be located in Mölndal, Sweden and reports to the Director of Clinical Affairs. For more information, please contact recruiting manager, Anna-Karin Lundgren, telephone + +46 31 3764278
Please note that we will review applications continuously, so be sure to send in your CV as soon as possible.
Welcome with your application! Visa mindre

Vill du vara en viktig del i hanteringen av råvaror, inleveranser och utleveranser för ett företag som arbetar med att göra skillnad varje dag.
Om rollen
I rollen som Warehouse worker kommer du att tillsammans med engagerade kollegor arbeta på både vårt lager MDC och på vår godshantering på Aminogatan. Du kommer i grunden vara på lagret MDC men det finns också en rotation mellan de två lagerverksamheterna. Arbetstiden är förlagd till dagtid.
Dina huvudsakliga arbetsuppgifter är:
Orderplock
Ansvara för in/utleveranser
Lagerhantering av råmaterial samt färdiga produkter inom Wellspect
Förse packavdelning med material och produkter
Hantering av våra olika truckar, skjutstativ, ledstaplare och motviktstruck som en naturlig del i ditt arbete.

Vem är du
Vi tror att du är en kvalitetsmedveten, flexibel och noggrann person som tar ansvar för ditt arbete. Du tycker om att ta egna initiativ och samarbetar gärna tillsammans med engagerade kollegor men kan också arbeta individuellt.
Vi vill att du har;
Gymnasieutbildning
Truckkort samt B körkort
Du kan utrycka dig väl i tal och skrift på svenska och gärna även på engelska
Datorvana är av stor vikt då arbetar dagligen med det i olika program

Det är meriterande om du har erfarenhet av lagerarbete, orderhantering och movex.
Bra att veta
För mer information, ring gärna rekryterande chef, Marie Hedberg, telefonnummer 031-376 32 18
Sista ansökningsdagen är 11 april 2021. Ansökningar kommer att hanteras löpande, så skicka in din ansökan snarast möjligt.
Om Wellspect HealthCare
Wellspect HealthCare, med huvudkontor i Mölndal i Sverige, är en ledande global leverantör av innovativa medicintekniska produkter och tjänster med fokus på hjälpa människor som lider av urinretention eller kronisk förstoppning. Varje dag arbetar mer än 1 100 engagerade medarbetare med att göra skillnad för de som behöver våra produkter och våra tjänster. Många av dem som vi hjälper har ryggmärgsskada, förstorad prostata, ryggmärgsbråck eller multipel skleros. Vi är en av världens ledande tillverkare av intermittenta urinkatetrar, med LoFric® som vårt mest kända varumärke. Som hjälp till de med kronisk eller svår förstoppning har vi utvecklat vad som sannolikt är världens mest avancerade irrigationssystem, Navina Systems™, vilket kombinerar en hög grad av användarvänlighet, klinisk effekt och kommunikation i ett verkligt smart system. Wellspect HealthCare är representerat i fler än 30 länder samt ingår i Dentsply Sirona, världens största tillverkare av professionella tandvårdsprodukter och teknologier med huvudkontor i North Carolina, USA. Företagets aktier är listade på amerikanska NASDAQ under symbolen XRAY. Mer information finns på www.wellspect.com och www.denstplysirona.com. Visa mindre

Vill du bli en del av Atlantis produktion? Vi söker nu en medarbetare för arbete inom ordermottagning, skeppning och skanning.
Om rollen
I rollen kommer du att hantera inkommande order som skall skannas och skeppas till kund.
Dina huvudsakliga arbetsuppgifter är att:
Granska, verifiera och registrera inkommande order i Atlantis ordersystem samt i Movex
Justera arbetsorder samt följa upp att dessa är korrekta eller åtgärda eventuella felaktigheter
Skanna gipsmodeller i en 3D skanner
Skeppa det färdigproducerade materialet till kund och avsluta kundorder


Vem är du
Vi tror att du är en flexibel, noggrann och självständig person som tar egna initiativ. Du trivs i en dynamisk organisation med högt tempo och krav på kvalité och service. Du är öppen, positiv och en god kommunikatör som har lätt för att samarbeta och skapa relationer.
Vi tror att du har:
Gymnasieutbildning
Minst två års erfarenhet av liknande arbete
Goda kunskaper i svenska och engelska, ytterligare språkkunskaper är meriterande
Datavana med goda kunskaper i Office-paketet samt har lätt för att lära nya mjukvaror
Förmåga att prioritera och fördela ditt eget arbete med en positiv inställning och känsla för service


Bra att veta
Tjänsten är en visstidsanställning med tillsättning snarast möjligt.
Arbetstiden är förlagd på en rullande 2 veckorsperiod där du ena veckan arbetar 07:55-16:33 och andra veckan 08:40 - 17.18.
För mer information, kontakta gärna rekryterande chef, Antonio Cucu via e-mail eller telefon:
[email protected] eller telefon: +46 702 219850.
Vår förhoppning är att tillsätta denna roll snarast möjligt, men vi föredrar att hitta rätt person snarare än att hitta någon snabbt.
Sista ansökningsdagen är 24 mars, 2021. Ansökningar kommer att hanteras löpande, så skicka in din ansökan snarast möjligt.
Om Dentsply Sirona
Dentsply Sirona är världens största tillverkare av tandvårdsprodukter och -lösningar, och har under 130 år erbjudit innovationer och service till tandvårdssektorn och patienter över hela världen. Dentsply Sirona utvecklar, tillverkar och marknadsför ett heltäckande utbud av produkter och lösningar för dental hälsa, liksom andra medicintekniska förbrukningsartiklar och har en stark varumärkesportfölj i världsklass. Som ”The Dental Solutions Company”, marknadsförs innovativa, högkvalitativa och effektiva lösningar för avancerad patientvård som ger bättre, säkrare och snabbare behandling. Dentsply Sironas globala huvudkontor ligger i USA, i York, Pennsylvania, och det internationella huvudkontoret finns i Salzburg, Österrike. Företagets aktier är listade på amerikanska NASDAQ under symbolen XRAY. Mer information om Dentsply Sirona och dess produkter finns på www.dentsplysirona.com. Visa mindre