Lediga jobb som Kvalitetsingenjör/-tekniker, kemiteknik i Mölndal

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture, and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives—and are made to feel valued, energized, and rewarded for their ideas and creativity.
AstraZeneca is also a leading pharmaceutical company focused on developing Active Pharmaceutical Ingredients (API) with advanced technologies. The Gothenburg facility employs digital solutions and automation to enhance production efficiencies.
As part of our commitment to innovation and collaboration, we are now offering a 6-month consultancy assignment through KellyOCG, with the possibility of extension. You will be fully integrated into AstraZeneca and report directly to your manager at AstraZeneca.
The arena:
The IT/OT Engineer will bridge the gap between IT and Operational Technology (equipment) in the manufacturing facility. Key responsibilities include maintaining IT systems that support business operations and manufacturing, ensuring system integrity and security, troubleshooting IT-related issues, and collaborating with various stakeholders to ensure compliance with industry standards.
Tasks and responsibilities / The role:
IT Infrastructure Management:
Ensure the performance and availability of IT systems.
OT System Support:
Align IT support with production needs.
Proactively address IT-related issues affecting manufacturing.
Cybersecurity Management:
Implement cybersecurity measures for IT and OT systems.
Staff training on security.
Data Integration & Management:
Ensure smooth data flow between IT and OT systems.
Develop interfaces for real-time data exchange.
System Administration & Troubleshooting:
Resolve IT incidents impacting operational efficiency.
Collaborate with vendors for advanced issues.
Vendor and Stakeholder Management:
Manage vendor relationships and service compliance.
Coordinate IT/OT project goals with internal teams.
Compliance and Best Practices:
Maintain GxP compliance and thorough documentation.
Lead system audits and validations.
Continuous Improvement & Innovation:
Evaluate and implement new IT/OT technologies.
Mentor junior staff and lead innovation projects.



Benefits:
• Opportunities for continuous professional development and training.
Performance Indicators:
• Maintain 99.9% uptime of IT/OT critical systems.
• Ensure rapid incident response and 100% compliance with regulations.
• Achieve high satisfaction ratings from stakeholders.
Core systems and equipment:
• High Bay Warehouse system – LAGE
• Clinical supply planning and execution System – SmartSupplies
• Building Monitor System – EMIL
• Scanners and container label printers
• Decommissioning system – Verilite
• Label Printers with servers
• GMP Lab Computers
Essential requirements:
Education: Bachelor’s in Computer Science or related field; OT/Cybersecurity certifications preferred.
Experience: 5+ years in IT with 2+ years in OT, especially in pharmaceutical manufacturing; experience with systems like SAP S4/HANA. Experienced in Power BI, Power Automate, MS Lists.
Skills: Strong knowledge of IT/OT convergence, excellent problem-solving abilities, and understanding of cybersecurity best practices. GMP knowledge.
Soft skills / Personal Attributes:
Effective communication, multitasking, attention to detail, and commitment to excellence.
AstraZeneca is one of the world’s most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that improve patients’ lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.
Last day to apply for this position is 15 May. Visa mindre

Are you ready to make an impact on the future of medicine? KellyOCG, a global talent solutions provider, is seeking a Quality Assurance Partner, on behalf of our partner, AstraZeneca. The 12-months long contract position (with possibility for extension) is based onsite in Gothenburg/Mölndal, Sweden, where you will be completely integrated with the AstraZeneca team, reporting directly to the onsite manager.


Quality Assurance Partner- Associate Director Validation
Join us in our Site Quality Team! We provide Quality oversight in the development of Investigational products and have the responsibility for Licence to Operate at our development site and play an important part in the commercialisation of new medicines. Development Quality is a Global group, with teams located in Gothenburg (Sweden), Macclesfield, (UK) and Durham (North Carolina, US). With a portfolio encompassing both small and large molecules, combination products and ground breaking technologies you will be a part of providing novel life-changing medicines to our patients around the globe.
Are you ready to take the lead in ensuring patient safety and maintaining License to Operate across our Development functions? As an Associate Director in Site Quality, you will be the prime source for quality/compliance advise in validation activities and provide quality leadership to Development functions. You will interpret AZ regulatory and GMP standards into appropriate quality standards and provide guidance to ensure AstraZeneca and Regulatory requirements are met. The role requires independent operation, risk management and lean skills, and decision-making against a background of varying regulations and standards. Your responsibility will extend to internal assets and GMP compliance decisions, having a major impact on AZ’s business.
Your role
As an Associate Director, you will develop and maintain in-depth knowledge of the quality regulations and guidelines applicable to your area. You will mentor and support junior colleagues, build strong customer relationships, and participate in GxP audits/initiatives. You will also be responsible for developing and approving GMP documentation and QA risk assessments, providing Quality input into business improvement projects, and be part of external Regulatory Authority GMP inspections. You will work closely with the leadership teams of our customers to set strategic direction for quality within that area, maintaining quality oversight and driving continuous improvement.
Most appreciated in the role is the ability to lead projects, to improve processes or ways of working and support different functions with your subject matter expert knowledge. Working in a development environment makes your role versified and enables lifelong learning in everyday tasks.
Essential for the role:
• Appropriate scientific degree with extensive experience (5-10 years) of working with validation, in a pharmaceutical GMP environment, preferably within a pharmaceutical development organization
• Extensive experience from working with all types of validation including, equipment, automation and IT system.
• A broad and comprehensive understanding of Quality Systems and GMP and good knowledge and reputation in the QA arena and specifically in GMP matters
• A comprehensive understanding of the pharmaceutical/drug development process is essential. A detailed scientific understanding of the Product types being supported is desirable
• Experienced in leading projects, making decisions, acting courageously and communicating with conviction and inspiration and in building excellent relationships both internally and with external suppliers or service providers
• Understanding of Supply Chain processes is desirable
Soft skills:
•You thrive when you work independently, when leading projects and take pride in structuring your day, knowing that the diverse workload can change the schedule with little notice.
• You are a problem solver who can look at solutions in a pragmatic way - coming up with creative solutions whilst still following our strict regulations.
• Excellent team working and networking skills
• Demonstrates independent judgement and uses risk management in complex situations
• Capable of making decisions, acting courageously and communicating with conviction and inspiration
• Demands excellence (sets high bar) and delivers
• A good communicator with experience of interacting effectively across interfaces


Latest application date is March 13th, but we review applications continuously, and could proceed with candidates before the last application date.
Why AstraZeneca
At AstraZeneca, we take Quality seriously. Our work is important, valued, and at the forefront of discovery, development, and commercialization. We are always innovating, trialing the latest models and technologies to improve reliability and excellence in our processes. We are proactive, science-based, and driven by our ambition to go far. We are a team of ambitious people who want to achieve. We work together as a team, get our pipeline out to patients sustainably, reliably, and safely. We follow evidence to reach outcomes that benefit patients and AstraZeneca.
Make a difference! Apply now and join us in our journey to push the boundaries of science and make a real-life difference to patients.
About AstraZeneca Gothenburg Hub
Our stunning campus in Gothenburg is one of AstraZeneca’s three strategic science centers. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we’ve built a series of environments where innovation can happen. Visa mindre

Are you ready to make an impact on the future of medicine? KellyOCG, a global talent solutions provider, is seeking a Quality Advisor (QA Specialist) on behalf of our partner, AstraZeneca. The 12-months long contract position (with possibility for extension) is based onsite in Gothenburg/Mölndal, Sweden, where you will be completely integrated with the AstraZeneca team, reporting directly to the onsite manager.
The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world’s leading pharmaceutical companies?
The Development Quality function is responsible for quality oversight of the pharmaceutical development activities within AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team.
AstraZeneca’s pharmaceutical development organizations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase
We have an exciting opportunity for a 12 months temporary assignment as Quality Advisor, in the Site Quality Gothenburg team, who’ll be the prime source for quality & compliance advice and providing quality support to the science functions and throughout the drug development process chains.
This is a great opportunity for you who are strong in quality and like to work close to development, Good Manufacturing Practice and making sure quality is assured when delivering new products.
The role
Working in the Site Quality team means you will work closely with the internal assets/facilities, teaming up with the pharmaceutical development functions and be involved in cross business processes. To build strong relationships with these functions knowing their business is key, to give support to projects and develop ways of working that builds for success.
The ability to interpret and trend compliance data to measure and improve quality standards is key. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting.
Whilst taking on your own specialist areas and making good quality decisions, you will be encouraged to think strategically and use your problem solving skills to resolve any quality issues. You will participate and contribute to continuous improvement projects with the aim to standardize and simplify our internal processes.
Typical Accountabilities:
• Responsible for quality release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
• Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects related to drug product
• Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
• Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working
Minimum requirements - Education and Experience
• MSc in pharmacy or engineering (specializing in Pharmaceuticals) with at least 3 years’ experience of working within a pharmaceutical GMP environment
• Demonstrates understanding of international quality systems regulations, concepts, industry practices to adopt best in class processes
• A comprehensive understanding of GMP regulations, the pharmaceutical development process and supply chain process would be advantageous
• Experience of interacting effectively across interfaces collaborating internally in a good communicative way
• Fluent in written and spoken English
Required soft skills:
• Ability to work in a fast-paced environment, meet deadlines, and balance multiple priorities. Independently motivated, detail-oriented, and "can-do" attitude
• Excellent team working and networking skills and encourages team effectiveness
• A good communicator with experience of interacting effectively across interfaces collaborating internally


Latest application date is March 13th, but we review applications continuously, and could proceed with candidates before the last application date.
About AstraZeneca Gothenburg Hub
Our stunning campus in Gothenburg is one of AstraZeneca’s three strategic science centers. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we’ve built a series of environments where innovation can happen. Visa mindre

Ansvarsområde
Som kvalitetstekniker kommer du att utföra slutkontroll och frisläpp av produkter samt se till att alla aktiviteter har utförts enligt gällande instruktioner. Du kommer bland annat att:
utföra kontroll av steril och icke-steril orderdokumentation
ingå i projekt för ständiga förbättringar
arkivera batchdokumentation

Bakgrund/Kvalifikationer
Vi tror att du är en positiv och driven lagspelare. Du är öppen för utmaningar och tycker om att arbeta tillsammans med duktiga och engagerade kollegor där varje dag gör skillnad.
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 från reglerad verksamhet
det är också meriterande om du är bekant med ISO 13485:2016 Medical Device – Quality Management System och FDA Quality System Regulation 21 CFR Part 820 eller har erfarenhet från medicintekniska produkter eller andra produktområden med höga regulatoriska krav
erfarenhet av att hantera mätinstrument såsom skjutmått, mikrometrar mm.

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
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 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

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

Are you interested in assuring safe and high-quality products from our suppliers all over the world? Is food and health something that gets you going? Then this is the position for you! We are looking for a Supplier Quality and Food Safety Specialist to the Supplier Quality team within the QEHS organization in the Paulig Group. In this role you will work with all our famous brands and products.
This position has the full responsibility of all Quality and Food safety related activities together with our suppliers and internal stakeholders. You will be in close contact with a group of suppliers to our company to assure the products and services they deliver meet our high standards and requirements as well as legislation and customer requirements. It is a central function in the company which means you will have a broad network of contacts within and outside of our company. Good communication skills and having an agile approach and enjoying a high pace is important to succeed in this role. If this sound like the perfect match for you, don’t hesitate to get in contact with us for questions or to send your application.
You will be part of an international team of 10 colleagues and will report to the Head of Supplier Quality. The position can be placed in any of our Paulig offices.
Job description
Work together with the Sourcing and Hedging function in the supplier approval process and supporting the selection of right supplier
Responsible to define and ensure right quality of raw materials, traded items and packaging material to meet the current legislations and regulations
Responsible for Supplier Questionnaire analysis and supplier risk evaluation
Responsible for planning and performing supplier audits, follow-up on results and drive implementation of corrective actions
Responsible for supplier performance improvements (non-conformances, remarks from supplier audits etc)
Responsible for supplier specifications, Quality and Food safety parameters
Keep documents and procedures within quality and food safety up to date
Supporting value engineering in relevant fields of expertise
Monitor and drive quality and food safety improvements in close co-operation with the suppliers and internal stake holders

Required knowledge and experience
Bachelor or Higher degree in food science or equivalent.
Experience in food manufacturing processes.
Experience in Quality and Food safety management systems.
Knowledge in Food safety audits at suppliers.
Experience in international food business
Food Safety regulation skills.
Ability to interpret and implement Food Safety legislation.
Good business acumen
Fluency in English.
Frequent travel is required in this role when performing supplier audits Visa mindre

Job description
Quality Assurance Advisor

 Are you interested in a challenging opportunity within the Development Quality function in one of the world’s leading pharmaceutical companies? 

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca. We are now looking for 3 Quality Advisors with GMP focus to our Gothenburg team. AstraZeneca’s pharmaceutical development organizations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.

Responsibilities
As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability.

You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role you will have interactions with internal and external stakeholders.

Typical Accountabilities:
Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities
Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects
Provide appropriate Quality Assurance input to business improvement projects
Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working.


Qualifications
Minimum requirements – Education and Experience
MSc in pharmacy or engineering (specializing in Pharmaceuticals) with at least 3 years’ experience of working within a pharmaceutical GMP environment
Broad understanding of Quality Systems and GMP and related activities to Investigational Medicinal Product (IMP)
Comprehensive understanding of the pharmaceutical/drug development process
Good communicator with experience of interacting effectively across interfaces
Understanding of Project Management processes
Fluent in written and spoken English

Preferred requirements
Experience preferably within a pharmaceutical manufacturing organization
Good team working and networking skills
Capable of making effective decisions
Demonstrate drive and energy in the role to make a difference
Demonstrate a high degree of personal credibility


Application
Deadline: 2022-04-29 , selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.

For more information:
Please contact Petra Govik [email protected] or Birgitta Nyström [email protected]

About the company
Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many activities.

Randstad Life Sciences specializes in the field of science and is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Do you want to be part of our competent team, contribute to high quality and also have fun while working? Join our team to make a real difference!

As a Quality Engineer, you will work in our Quality Assurance department and make sure that we are in compliance with regulatory directives for Medical devices. You will not only handle existing products but also be part of a cross functional project team and have the opportunity to have a key role in the development of our future products. In this role you will also face many different functions within the company and you will have the opportunity to grow into an important player in our projects.

Key Responsibilities
Review and release of batch documentation / device history records.
Non-conformity handling.
Review and approval of change notifications.
QA support to product / engineering changes and product development projects
Validation activities.


Requirements and Qualifications
Master´s or Bachelor´s degree in engineering, science or technical discipline
at least 3 years of experience within Quality
a strong drive to achieve goals and targets
documentation and communication skills, in English as well as in Swedish
We think you are a positive team player. You are open to challenges and enjoy working together with highly skilled and committed colleagues. You have high integrity and a strong performance drive as well as a wish to look into new ways of working.


We can offer you an exciting and challenging job in a company that is committed to make a real difference every day. This position is located at our headquarter in Mölndal, Sweden.


For more information, please contact recruiting manager, Pia Hindrichsen, telephone +46 767 619547.

Please apply no later than November 1, 2020. Please note that we will review applications continuously, so be sure to send in your application as soon as possible.


About Wellspect
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

Do you want to work in a global organization and providing better dental care to make people smile?


About the position
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 to Design Reviews and actively be part of development and establishment of a robust process with appropriate Quality Control Measures.


Your key accountabilities are:
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


Who you are
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.


We believe you have:
Master or Bachelor degree in engineering, science or technical discipline
at least 3 years of experience within Quality Assurance
experience from measuring machines and instruments
it is considered as 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 medical device or other product areas with high regulatory demands
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



Good to know
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 30th of September 2020. 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 solution 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