Lediga jobb som Forsknings- och utvecklingschefer i Mölndal

The Team Leader for Research Services Quality Labs (AST & Cell Bank Support) is responsible for the day-to-day operational management and leading the associates of the Research Services Quality Labs team at an Avantor Services customer site. The team directly and indirectly support researchers in various functions and departments at AstraZeneca Gothenburg. With the aim to deliver sustainable, integrated laboratory services, the Team Leader is driving service excellence through engaged and enabled team members. Reporting to the Avantor Services Research Services Quality Labs Service Manager, the role will be responsible for the quality and performance of Research Services Quality Labs Team within the labs and their development in accordance with customer requirements and legislation utilizing LEAN principles. Together with the team and colleagues the Team Leader will work with a wide range of contacts including customers, suppliers, logistics and commercial colleagues, maintaining a consistently high level of customer focus to achieve our strategic objectives. The role is multifaceted, and both based on and off lab and must be performed in a safe, regular and work environmentally correct manner.
Focuses on people-centered leadership, performance, and lab innovation.
Responsibilities:
Lead and manage a team of Avantor Services on-site associates, helping them perform at their best, through motivating and developing them to achieve high performance and developing succession plans.
Assisting the Research Services Quality Labs Manager in planning the aims, objectives and priorities of their work area (and communicating this to the team and to colleagues as appropriate).
Accomplishes human resource objectives by recruiting, selecting, orienting, training, assigning, scheduling, coaching; communicating job expectations; planning, monitoring, appraising, and reviewing job contributions; On the other hand, the T Enforcing policies/procedures.
Delivering 'value' for the client by constantly developing the performed services through innovation.
Establishing and maintaining risk and quality, ensuring performance and compliance targets are met.
Actively partner with other outsourced FM service providers, ensuring a seamless customer experience.
Ensure that all environmental, health and safety related aspects (and required trainings) are in line with both customer and Avantor expectations.
Creation, maintenance and updating relevant documentation in support of service delivery, compliance and training.
Lead and manage minor projects related to specific business area.
Reports on KPIs, relevant metrics, SLAs in line with contractual agreement.
Solve problem and maintain an open communication with scientist and managers at AZ.
Maintain a clean, tidy and organized workspace.
Follow all health, safety, and environment requirements that are defined in the work instructions and communicated in various educations.
Ensure that AZ company policies, guidelines and standards are in compliance.
Participate in or lead dialogue and meetings with customers.

Accountabilities
Lead and manage the team consisting of Lab Manager, Operational Lead, In vivo Techs, Cell bank Coordinators/Specialists that is partly responsible for the daily operational work within Research Services Quality Labs
Ensure associates are fully trained and informed of the work tasks and regarding the lab environment they work within.
Lead the Research Services Quality Labs team within the labs.
Actively drive and deliver change into the operation to ensure the support is aligned with the customer needs.
Proactively identifies and implements efficiency and process improvements.
Build relationships with key stakeholders and suppliers to provide a collaborative approach with the operational associates in the lab space.
Meet regularly with relevant internal and external stakeholders to review new opportunities and performance delivery.
Ensure development of competencies and procedures in order to maintain an updated and smooth business.

QUALIFICATIONS
A bachelor's degree in a scientific discipline or equivalent experience.
Experience working in a laboratory environment with previous proven management and leadership.
Experience working with SHE policies and procedures.
Experience in working with quality assured processes and documents.
Knowledge about GMP, GLS and ISO standard requirements.
Knowledge of audit requirements.
Practical knowledge and experience of lean sigma processes.
Knowledge of SHE requirements in a laboratory environment and preferably a certification.
Speaking and writing both Swedish and English without any hindrance.
Used to and comfortable with computer-based work (skills in most Microsoft Office applications and e-mail).

KNOWLEDGE, SKILLS AND ABILITIES
Excellent customer service focus and ability to work collaboratively.
Ability to influence people at all levels to deliver improvements and cost savings to the customer.
Able to partner with other teams and suppliers and deliver results in a matrix environment, managing multiple internal and external partners/stakeholders.
High problem-solving capabilities and confidence to make clear decisions sometimes with limited information.
High level of planning, organizational, analytical and networking skills.
Project management skills, ability to be flexible and handle multiple responsibilities and tasks on a regular basis.
Self-starter, highly motivated with a strong bias for action/execution.
Self-motivated, energetic, dependable and with a clear attention to detail.
Exceptional communication skills and ability to converse at all levels.
Personal Impact – skilled at getting individuals behind an aligned purpose; acts in line with a visible set of values and beliefs; comfortable to work through conflict with an ability to see a positive outcome in difficult situations.
A good team worker demonstrating loyalty and commitment to the organization and team members.
Careful and orderly with a very high regard for safety.
Ability to work independently as well as in a group.
Problem solving attitude.
Respect and understanding for laboratory work.
Strong working ethic.
Service-oriented and social.
Good prioritization skills with the ability to maintain several processes at once. Visa mindre

Avantor is currently looking for a Laboratory Manager to join the growing team in Mölndal, Gothenburg! In this role, you'll manage the day-to-day operations of the biological laboratory, acting as the primary contact for Laboratory Users. If you’re eager for a new challenge in an international environment with a strong scientific background and excellent people skills, this could be the opportunity for you!
This is a full-time, temporary (12 months) position based in Mölndal, Sweden - a hub for drug development and pharmaceutical production. Along with an attractive salary, we offer multiple benefits, including a bonus, pension scheme, private medical care, and more!


Working hours: Monday - Friday, flexible start times between 6:00am - 9:00am, with finish times between 3:00pm – 5:00pm. You’ll need to be on-site from 9:00am – 3:00pm, with flexibility for the remaining hours to be worked from home or in the office.


The team
You’ll be part of a team of 11 associates, including Laboratory Managers, Laboratory Technicians, and Research Technicians, working in an open, supportive environment within the Lab & Production Services department. This team supports pharmaceutical companies and laboratories worldwide in Life Sciences R&D.


What we’re looking for
Education: A Bachelor’s or Master’s degree in a scientific discipline.
Experience:
Hands-on laboratory experience, leadership in lab improvements, and project management
Experience in large-scale laboratory settings
Previous experience at a senior laboratory technician level or above in a multi-disciplinary laboratory environment

Skills:
Proficiency in MS Office and willing to learn new digital skills
Excellent communication skills in English and Swedish, confidence in communicating with people from various seniority levels
Proven ability to partner with other teams and suppliers, delivering results in a matrix environment
Experience managing multiple internal and external partners/stakeholders
Knowledge of SHE requirements and GxP regulations



Key Responsibilities
Manage laboratory’s operations, serving as the primary contact for scientists on materials flow, facilities maintenance, equipment availability, and process optimisation
Maintain laboratory operational efficiency by coordinating with facility maintenance suppliers and scheduling maintenance with minimal disruption
Resolve queries such as broken equipment, out-of-stock consumables, and alternative product sourcing
Lead continuous improvement projects focused on equipment, change control, and optimising people processes
Investigate deviations from Service Level Agreements (SLAs) through root cause analysis and accurately report findings Visa mindre

Job Description
Avantor is currently looking for a Lab Manager in ECD to join the growing team in Mölndal, Gothenburg! In this position, you are responsible for the day-to-day operational management of your defined set of laboratories, supporting the Early Chemical Development (ECD) group. ECD is a world class CMC department with responsibility for early phase drug substance. You will act as the first point of contact for Lab Users and much more! Are you looking for a new professional challenge in an international environment and do you have a chemical engineering or chemistry background? Are you a people-person with a lot of energy and drive? Then this might be the opportunity for you! - Let’s talk!
This role will be a full-time, permanent position, based at our customer site, AstraZeneca, in Mölndal. Next to an attractive salary, we offer multiple benefits such as a bonus, pension scheme and Health Care allowance. You get to establish a solid network within the industry, by collaborating with multiple different stakeholders and you get to contribute to a growing team.
Working hours: Monday - Friday, flexible start time between 6:00 - 9:00 and finish time 15:00 - 18:00
The team
The Lab Manager ECD is the first point of contact for three units composed of five teams, and gets to work in an open and supportive environment. This team belongs to our department Lab & Production Services, which supports leading pharmaceutical companies and laboratories all over the world, in Research and Development within the Life Sciences industry.
What we’re looking for
Education: Master’s degree in Chemical Engineering, Process Engineering or Chemistry
Experience:
Hands-on lab experience leading lab improvements and coordinating lab installations, is required
In Project leadership and/or working in large scale lab environment is a plus

Preferred Qualifications:
Good MS Office knowledge and willing to learn new digital skills
Understanding of working under the ATEX European Directives
Effective communication skills in English and preferably in Swedish
Flexible, good in setting priorities and strong in dealing with ad hoc requests
Strong time management skills, pro-active and outgoing
Flexible, stress resistant and able to deal with multiple priorities
Confident, able to lead meetings and to present to bigger groups

How you will thrive and create an impact
Act as the single point of contact for the assigned laboratories and handle ad hoc questions / issues of lab users
Organize and lead regular lab user group meetings and lead any actions as required
Ensure the laboratory maintains its operational efficiency by planning preventative and scheduled maintenance regimes with minimal impact to daily operations
Liaise with AstraZeneca’s Facility Management team and actively participate in the CAPEX process
Actively participate in Risk Assessments of incoming instruments following the ATEX European Directives
Assist in creating and updating work procedures for various assays, particularly focused on reagents/consumables and cost saving recommendations.
Manage training of lab support staff working in the area to ensure all are working to a consistent level
Assist with organized visits from internal/external partners
Introduce new staff working in the laboratory
Provide operational support on projects to build understanding of business needs and identify opportunities for process improvements
Create, maintain and update relevant documentation in support of service delivery, compliance and training



#LI-Onsite Visa mindre

Avantor is currently looking for a Lab Manager Chemistry to join the growing team in Mölndal, Gothenburg! In this position, you are responsible for the day-to-day operational management of your defined set of laboratories, you deal with ad hoc questions and problems, act as the first point of contact for Lab Users and much more! Are you looking for a new professional challenge in an international environment and do you have a chemistry background? Are you a people-person with a lot of energy and drive? Then this might be the opportunity for you! - Let’s talk!
This role will be a full-time, permanent position, based at our customer site, AstraZeneca, in Mölndal. Next to an attractive salary, we offer multiple benefits such as a bonus, pension scheme and Health Care allowance. You get to establish a solid network within the industry, by collaborating with multiple different stakeholders and you get to contribute to a growing team.
Working hours: Monday - Friday, flexible start time between 6:00 - 9:00 and finish time 15:00 - 18:00
The team
The Lab Manager Chemistry is the first point of contact for four different laboratories and gets to work in an open, supportive team. Together with four other Lab Managers, you are part of the Chemistry and Automation team, currently counting 10 associates in total. This team belongs to our department Lab & Production Services, which supports leading pharmaceutical companies and laboratories all over the world, in Research and Development within the Life Sciences industry.


What we’re looking for
Education: Master’s degree in sciences, preferably related to Chemistry
Experience: Hands-on lab experience is required, this can also be from internships
Preferred Qualifications:
Good MS Office knowledge and willing to learn new digital skills
Effective communication skills in English; Swedish is a plus
Flexible, good in setting priorities and strong in dealing with ad hoc requests
Strong time management skills, pro-active and outgoing
Flexible, stress resistant and able to deal with multiple priorities
Confident, able to lead meetings and to present to bigger groups



How you will thrive and create an impact
Act as the single point of contact for the assigned laboratories and handle ad hoc questions / issues of lab users
Organize and lead regular lab user group meetings and lead any actions as required
Ensure the laboratory maintains its operational efficiency by planning preventative and scheduled maintenance regimes with minimal impact to daily operations
Assist in creating and updating work procedures for various assays, particularly focused on reagents/consumables and cost saving recommendations.
Manage training of lab support staff working in the area to ensure all are working to a consistent level
Assist with organized visits from internal/external partners and regulatory bodies
Introduce new staff working in the area to the laboratory
Provide operational support on projects to build understanding of business needs and identify opportunities for process improvements.
Work with IT/other service providers to ensure equipment is running effectively, scientists have what they need
Liaise with scientific equipment responsible to manage equipment breakdowns, servicing and planned maintenance
Create, maintain and update relevant documentation in support of service delivery, compliance and training.
Report on KPIs, relevant metrics, and weekly tasks.
Organize and lead lab group meetings



#LI-Onsite Visa mindre

Job description
Supply Chain Manager for Clinical Trial medications


Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.


We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca’s trials all over the world. Our goal is to never miss a patient. In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.


This is a consulting assignment with Randstad Life Sciences. 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 social activities.

Responsibilities
Your main responsibilities will include:
• Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply.
• Ensure effective communication with project teams and key partners across a global network.
• Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
• Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
• Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
• Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.


About randstad life sciences
Randstad Life Sciences is specialized in competencies 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.


Deadline: 2024-05-03, selection and interviews will be ongoing. For more information: Please contact Katan Ali, [email protected]

Qualifications
What you'll do:


In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.


To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.

About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Tork is the #1 brand for professional hygiene solutions, and we are the global market shaper. We are a 3 billion-dollar B2B brand that’s part of a $14B hygiene company called Essity, a leading global health and hygiene company with sales in over 150 countries and over 36,000 employees.
We create, manufacture, market, and sell everything from soap and sanitizer to toilet paper, hand towels and napkins and everything in between. Our products and services are sold in over 100 countries around the world with leading market positions in most - and we’re growing every day.
We are a team driven by the Tork brand purpose to deliver “sustainable hygiene for all”. We care deeply about the well-being of all people and the planet we live on. We are a diverse, successful, and collaborative team with a passion for making the world a safer, cleaner, and better place. At Tork we push ourselves to explore and develop on the leading edge of Marketing, Branding, Innovation, and Digital technology. If you are as eager as us to learn, develop and help create the future of professional hygiene while contributing positively to society, then we need to talk!
About the Role
We are looking for a leader who is an entrepreneurially-minded person with a passion for and experience in delivering impactful innovation. This person will contribute to the overall innovation strategy and will be leading the tissue/refill development of the future toilet solution for away-from-home washrooms that not only help our customers to improve people’s well-being but also help save our planet.
As a Global Technical Innovation Manager, you will lead the technical development of innovations around the world with a focus on the tissue/refill part of the toilet paper systems. You will work in a marketing / technical partnership to lead prioritized concepts through all stages of the innovation funnel. This is done in close cooperation with multiple key stakeholders (global technical innovation manager for dispensers, global brand director, R&D, manufacturing, customer insights team, and the regional/local product organization), to grow the Tork brand. The role is reporting to a Global Innovation Director in Professional Hygiene, located in Gothenburg (Sweden).
We’re looking for people who embody our values and aren’t afraid to challenge, innovate, experiment, and move at a fast pace. We’re always looking for ways to improve our products and ourselves. If this is you, we’d love to talk.
What You Will Do


Contribute to and implement the toilet solutions strategy for Professional Hygiene, with a focus on the technical area related to the tissue/refill part of the solution.


Input into overall product strategy and assortment vision to the Global Brand Director.


Secure a good customer understanding and translate it into the technical requirement.


Lead the technical feasibility of the tissue/refill part in the projects based on customer insights.


Own the tissue/refill specifications within a targeted area.


Lead and act as project manager for innovation projects through all stages of the innovation funnel.


Propose Innovation project organization and resources.


Collaborate closely with the Global Technical Innovation Manager for dispensers, R&D team and Global Brand Innovation Managers to drive projects forward.


Collaborate closely with the Global Brand Director, Product & segment marketing teams, Customer Insights, R&D, Manufacturing, Regulatory and multiple other functions in our highly matrixed organization to create, develop, optimize and bring to life innovations with a sense of urgency and purpose.


This position will ideally be located in one of our main hubs; Gothenburg, Colmar, Munich or Philadelphia.

Who You Are


A deep passionate for innovation and someone eager to contribute to the transformation of Toilet Solutions


At least 5 years of experience in technical development and/or innovation management. Experience in the tissue area is a plus.


Ideally with experience in Product Design, Process Engineering, Chemistry, or Mechanics.


A supreme task/project manager who sweats the details and is comfortable with project management tools to keep things on track.


An entrepreneurial spirit – you are a strong strategic thinker and appreciate process but are more concerned with delivering results and aren’t afraid to roll up your sleeves and get things done.


A holistic thinker – you can see the big picture and connect dots others don’t.


A collaborative leader – someone who drives results and is a team player.


Able to influence and get the buy-in of key stakeholders in a global matrix organization and effectively manage work across organizational boundaries to get things done collaboratively with high resilience and a solution-oriented attitude.


Able to embrace diversity and work in multicultural environments.


Speak English fluently.

Don’t believe that you meet every single requirement? That’s ok. We encourage you to apply anyway!
We are dedicated to building a diverse, inclusive, and authentic workplace. So, if you are excited about this role but your experience does not align perfectly with every qualification in the job description, please apply! You may just be the right candidate for this or other roles here at Essity.

What We Can Offer You
You’ll have a chance to help shape the future of hygiene in a way that breaks the paradigm between sustainability and efficacy.
At Essity, we believe everyone's learning and professional development is unique and want to empower employees to reach their full potential in a winning culture motivated by a powerful purpose.


Collaborative and Inclusive Culture | Empowering & Engaged Leaders | Working with Powerful Purpose & Sustainable Impact | Learning and Growing in your Career | Supporting Well-being & Sustainable Working Life | Life-changing Innovations | Competitive Total rewards Visa mindre

Avantor is currently on the lookout for a Lab Manager for our cell Laboratory in Mölndal! Are you a people-person with a lot of energy and drive? Do you like being a spider in the web? Then this might be the opportunity for you!
As a Laboratory Manager you will be responsible for the day-to-day operational management of the cell Laboratory, you deal with ad hoc questions and problems, act as the first point of contact for Lab Users and much more! Are you looking for a new professional challenge in an international environment and do you have a scientific background? Let’s talk!
This role will be a full-time and permanent position, based at our customer site, AstraZeneca, in Mölndal (Gothenburg). You’ll work form Monday to Friday, with flexible working hours and no shifts. Next to an attractive salary, we offer multiple benefits such as bonus, pension scheme and Health Care allowance.
The team
The Lab Manager is the first point of contact for the Cell lab and belongs to a team of 8 associates, this role included. This team belongs to our department Lab & Product Services, which supports big pharmaceutical companies and laboratories all over the world, in Research and Development within the Life Sciences industry.
What we’re looking for
Education: Master’s degree in (Cell) Biology or related
Lab experience is required, this can also be from internships
Cell work experience is a great asset
Good MS Office knowledge
Strong communication skills in English; preferably good in Swedish, though this is not required

Who you are
Flexible, stress resistant and able to deal with multiple priorities
Able to work indecently, though also a great team player with a focus on team results
Attention to detail, organized and outgoing
Customer minded, driven and analytical

How you will thrive and create an impact
Act as the single point of contact for the cell lab and handle ad hoc questions / issues of lab users
Review the training of lab support staff working in the lab
Introduce new associates to the lab and procedures
Ensure the laboratory maintains its operational efficiency by planning the maintenance of lab equipment and by contributing to improvement projects
Collaborate with suppliers to investigate deviations and report back on them
Assist with site visits of both internal and external partners
Organize and lead lab group meetings
Provide operational support on projects to build understanding of business needs and identify opportunities for process improvements
Create, maintain and update relevant documentation related to procedures, training etc.
Work with the scientists to identify future requirements and new innovations in technology Visa mindre

We are looking for an Associate Director/Team Leader to join our MolecularAI (MAI) department. MAI drives the science, build the platforms and impact projects in applying ML/AI to drug design. The department also supports chemistry automation (iLab), oligonucleotide therapies and Open Innovation. The role will be based at AstraZeneca in Gothenburg, Sweden and in this role you will be part of the Discovery Sciences organization, working within a first-class scientific environment to support drug discovery across each of AstraZeneca’s therapeutic Areas.
At AstraZeneca, we’re not afraid to do things differently. We’re building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening up new ways to work, pioneering cutting edge methods and bringing unexpected teams together.
What you’ll do:
As an Associate Director Molecular Design in the MAI department, you will lead a multidisciplinary team of data scientists and ML/AI experts delivering ML/AI tools related to molecular de novo design to AstraZeneca drug projects, maximizing individual talents and developing a high-performing team by role modelling and leading by example. You will have a passion for scientific delivery and innovation, developing science and technology strategy and shaping the future of the MAI capability, and building trusted relationships with senior scientific colleagues. You will develop and maintain a high level of science and technology knowledge, building specialist expertise in molecular de novo to lead your team effectively, providing guidance, training and development. As well as make an active contribution to the development of the MAI department through leadership of multi-disciplinary initiatives that deliver value and impact to drug discovery projects.
Essential in the role:
· Extensive experience in method development related to molecular de novo design.
· Demonstrable great experience in applying molecular de novo design to drug discovery projects.
· PhD or equivalent in a relevant discipline.
· Experience in key stakeholder management.
· Experience of project management, team working, influencing and networking in a matrix organisation.
Desirable in the role:
· Experience of developing people to maximise talent and ensure high performing teams.
· Ambition to drive the science forward in applying molecular de novo design to drug design.
· Relevant publication record and experience of presenting scientific data.
If this sounds like your next challenge – apply now! Visa mindre

Job description
Supply Chain Manager for Clinical Trial medications


Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.
We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca’s trials all over the world. Our goal is to never miss a patient.
In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.


This is a consulting assignment with Randstad Life Sciences. 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 social activities.

Responsibilities
What you'll do


In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.
To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.


Your main responsibilities will include:
• Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply.
• Ensure effective communication with project teams and key partners across a global network.
• Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
• Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
• Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
• Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.

Qualifications
Essential for the role:
• Bachelor’s Degree in Supply Chain, business or scientific subject area – equivalent experience within Supply Chain will be considered
• Experience within a Supply Chain Management environment with a holistic knowledge of end-to-end supply chain activities (minimum 2 years experience desirable)
• Proficient IT skills with an ability to adapt and operate in bespoke multiple systems
• Experience in running projects and in?uencing customer demands
• Experience of demand planning and forecasting and risk identification and management
• Excellent English written and verbal communication skills


Desirable for the role:
• Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Lean knowledge and understanding
• Experienced in handling Quality Events (Deviations, Change Controls, Complaints)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Working in a leading role within a team

About the company
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

We are looking for you, an Engineering Manager who wants to be a part of a global high-tech product company, and who will coach, empower and engage our people!

About the position
As an Engineering Manager you will be a part of our Engineering Management Team which today consists of one Director Engineering, three other Engineering Managers and lead roles for system architecture and SAFe/Scrum. The Engineering Management Team reports to our Director Engineering.

The Engineering department consists of about 50 engineers working in a Scaled Agile Framework (SAFe) environment within embedded systems, system software as well as windows applications and web services.

You will be the manager of 8-16 people who may come from different agile teams. The overall responsibility as an Engineering Manager will be to coach, empower and engage individuals and your teams to reach their highest potential and to maximize customer value. You will manage performance appraisals, expectations, and compensation to stimulate personal development and performance.

In this role you will:
Align, anchor and execute on our strategy and roadmap.
Collaborate with managers and leaders (Product Managers, Product Owners, System Architects) to provide the best conditions for teams and individuals to thrive and to perform.
Evaluate performance and administer compensation, benefits, promotions, and corrective actions.
Attract, develop, and retain the best talent for teams according to business strategy and relevant emerging technologies.
Support teams and individuals with problem identification, root cause analysis, and decision-making. Delegate and prioritize tasks as needed.
Live, lead and create good examples according to our company values and policies.
Create a culture of innovation and continuous improvement.
Ensure strong collaboration between departments, teams, and individuals.
Handle Change management.
Assist in product planning and execution (including SAFe/Scrum ceremonies and events)
Build partnerships with suppliers, consultants, partners, internal and external stakeholders.

We are looking for you
.. who are into both technology and people and who want to create the best environment for your team to be able to work against the strategic goals. You engage your team to preform their best and make sure that they thrive. Your way of communicate is both persuasive and influential.

To be successful and thrive in this role we think that you have:
An educational background in business, engineering or similar
Around two years' experience as a manager or leader.
Change management experience.

It is a plus if you have experience in DevOps and/or Scrum/SAFe environment.

About us
Kollmorgen is a global company which develops motion control and Automated Guided Vehicle (AGV) systems and works with customers in many different industries all over the world.

Kollmorgen Automation is a part of Kollmorgen and we have our Swedish headquarter in Mölndal. The target is to provide world leading technology for the rapidly growing market of AGVs and Mobile Robots. The about 100 employees are working with product development, professional services, sales, marketing and finance.

Some of the good things that we offer
Innovation Days every twelve weeks - a 24-hour event for the whole company to dig deeper, explore new areas and solve problems! ????
Gym at the office filled with machines for strength and fitness that is always open and free to use for all our employees ????
Free parking outside our office ????
Noise cancelling headphones and home office equipment (office chair, screens etc) ????
Career opportunities within the company - we have employees who have worked with us for many years in different roles and departments ????
Day of Caring - every year we take one day to clean the west coast beaches together ?????
6 weeks’ vacation! ????
Work time reduction - it gives you around 7 extra days off per year
Collective agreement, occupational pension, wellness allowance

A part from above, Kollmorgen is characterized by an entrepreneurial spirit where you get the opportunity to carry out your ideas with the help of the company's experts.

We focus on engagement and personal development as essential tools for our success. We give you the opportunity to work in an open environment where ideas and thoughts are lifted freely among colleagues.

Additional information
Full-time employment.???? Based in Mölndal, Sweden. We recruit based on our values and for us it is important that you continuously want do develop yourself together with us!

Selection takes place on an ongoing basis, so send your application as soon as possible. Welcome with your application!

Check out more open positions (https://career-agv.kollmorgen.com/jobs),
? follow us on Facebook (https://www.facebook.com/kollmorgen.ndc),
get to know us better through our Candidate Blog (https://kollmorgenagv.teamtailor.com/blog),
? and see videos about our products at our Youtube channel! (https://www.youtube.com/user/ndcsolutions) Visa mindre

Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than January 31st, 2022.

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected].

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than January 31st, 2022.

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected].

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

To deliver on our commitments, we are looking for people with both broad and deep experience in clinical drug development as well as project management.

As a Clinical Trial Assistant, you will be responsible for coordination in and administration of our clinical trials. The role may also include overall administrative support in driving our business forward. The position will be located in our office in Uppsala or Mölndal.

Main responsibilities:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements).
- Attend project team meetings and generate meeting minutes.
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor


Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Collaboration skills in order to engage with people and clients
- Proven administrative skills
- Excellent knowledge of spoken and written Swedish and English


More information

For more information about the position, please contact Emilia Larsson, +46 76-111- 0659, or [email protected].

Please submit your application via this link with a short personal letter and your CV included, no later than 31st October, 2021. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical
At Antaros Medical, we are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We currently have around 90 employees working at our offices in Mölndal and Uppsala. Visa mindre

Do you want to be a part of a company that is committed to make a difference every day? The research and development (R&D) -function within Wellspect HealthCare is looking for a new manager. Join our team where we bring out the best in people in our effort to make a difference.


As the Head of System and Digital Products at R&D, you are accountable for driving development and maintenance of system-related and Digital products. You manage a team with goal to increase the digital product assortment within Wellspect.
As part of the R&D management team you actively participate in developing the whole R&D function.

Responsibilities:
Lead the System and Digital products-team of approximately 6 people through planning, execution and management of all operational aspects and budget
Plan, organize, direct and control the System and Digital products-team within appropriate guidelines, policies and regulations.
Contribute actively to project progress by adequate staffing, recruiting, competence building, and employee development.
Source and lead external partnerships
Manage the technical maintenance for the System and Digital products, over their life cycles.
Active member of the R&D management team in strategic planning, overall budgeting and staffing, and execution of these to ensure delivery of the organization’s responsibilities.



Qualifications / Background:
a Master of Science within Electrical engineering
a background with relevant experience of management from the Med Tech industry
a strong focus on product development and product maintenance of digital products
a proven track record of successful leadership skills
great time management skills and ability to prioritize and multitask
excellent communication and writing skills in English. Knowledge of Swedish is desirable.


Experience from several companies/organizations is considered a merit.

Our potential new colleague should have a winning attitude, able to self-start with a strong sense of accountability and urgency. You can develop relationships with all relevant stakeholders in a matrix organization as well as external partners and therefore enjoy both execution and collaboration. Being an inspiring leader, you coach your team to drive development and maintenance of System and Digital products within Wellspect.


You will report to the Vice President R&D and placed at our headquarter in Mölndal, Sweden.

For more information, please contact recruiting manager, Eva Wahlberg, Vice President of R&D phone +46 702 799219.

Please apply no later than January 31, 2021. Please note that we will review applications continuously, so be sure to send in your application as soon as possible. Visa mindre

Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in Swedish and English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than 18th July, 2021.

For more information about the position, please contact Richard Olbe, Manager Clinical Operations, at +46 732301011.

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre