Senior QA Scientist

We are looking for a Senior QA Scientist to join our team.

Are you passionate about quality assurance and scientific excellence in the field of cell therapy? Novo Nordisk Foundation Cellerator is seeking a proactive and experienced Senior QA Scientist to join our team. In this role, you will ensure patient safety, product quality, and compliance with GMP guidelines, while fostering a collaborative and inclusive work environment.

Novo Nordisk Foundation Cellerator is advancing the cell therapy ecosystem in Denmark by establishing and operating a state-of-the-art process development and GMP manufacturing facility in Lyngby just north of Copenhagen. The mission is to accelerate the progress of cell-based therapies toward clinical trials globally for the benefit of patients in need of novel cell therapies to treat and cure serious conditions. Cellerator will operate as a philanthropic entity dedicated to the development and manufacturing of cell-based therapies, serving both academic institutions and the industry alike.

The Job 

You will be part of the quality team which is a small team with both junior as well as very experienced people. In this position you will be the system manager of our electronic Quality Management System (eQMS). You will help in the mapping of quality processes, and you will have a leading role in the testing and documentation of the eQMS. You should expect the job to develop over time. In the first 1-2 years the system manager role will take more time until the eQMS is fully established. After that you should expect to spend more time on general QA tasks.

eQMS System Manager Responsibilities

• Maintain lifecycle documentation (URS, validation plans, SOPs) for the electronic Quality Management System (eQMS).
• Ensure system changes follow formal change control procedures and approve related policies.
• Support system validation and maintain validated state.
• Approve user access, maintain user groups, and conduct periodic access reviews.
• Responsible for conducting periodic access reviews.
• Act as the primary liaison with the eQMS supplier and support user onboarding and training.
• Participate in system reviews and risk assessments.
• Supports during audits and inspections
• Support training and onboarding of system users

General QA Tasks

• Manage training documentation and support training activities.
• Review and approve qualification protocols, reports, and production documentation (e.g., master and executed batch records).
• Represent QA in risk assessment workshops.
• Evaluate and approve GMP changes, deviations, SOPs, and analytical method procedures.
• Participate in supplier and material qualification processes.
• Review and approve analytical method procedures, analytical method qualifications.
• Participate in the qualification of new suppliers and new materials.

About you

We imagine you have:

• Industry experience (pharma, biotech, CDMO, CRO): MSc/PhD with 5–8 years, BSc with 8+ years.
• Proven experience with Good Manufacturing Practice (GMP) is required.
• Experience with IT in a pharmaceutical context and electronic QMS systems (system manager experience is an advantage).
• Deep understanding of cGMP, regulatory requirements, and QMS development.
• Experience in equipment/facilities validation and IT application validation lifecycle.
• QA liaison experience with suppliers, CMOs, or CROs is preferred.
• Knowledge of cell therapy drug development/manufacturing and stem cell biology is an advantage.
• Lead auditing experience is a plus.
• Strong written and oral communication skills, with the ability to convey complex content across organizational levels.
• Advanced IT skills, including MS Office and collaboration/project tools.
• Experience in international and cross-cultural/global teams is an advantage.
• Fluent in English, both written and spoken.

As a member of our team, you will be in a dynamic and rapidly evolving field, where new challenges and opportunities arise regularly. The job requires you to take initiatives and think out of the box. You have strong collaborative skills and the ability to build good relationships with the people around you. You are purpose driven and curious and eager to contribute also beyond your professional domain. And importantly, you are a doer – a person who gets things done.

At Novo Nordisk Foundation Cellerator, we offer more than just a job — we offer the opportunity to be part of something bigger. When you join our team, you'll become part of a dynamic and purpose-driven environment focused on accelerating life science innovation in Denmark and beyond. 

Here's what you can expect

• A High-Impact Role: Join a fast-paced, mission-focused team working at the intersection of science, business, and innovation. You'll collaborate with leading figures from the Danish life science ecosystem as well as influential European and global partners.
• A Value-Driven Culture: Be part of an organisation rooted in the Novo Nordisk Foundation's strong values. We are deeply committed to fostering a diverse, equitable, and inclusive workplace where all employees feel supported, respected, and empowered to thrive.
• Flexibility and Growth: We offer a flexible working environment that supports your personal and professional development. From individual learning opportunities to team-based innovation challenges, your growth is our priority.
• Attractive Compensation & Benefits: Enjoy a comprehensive benefits package designed to support your well-being — including competitive salary, pension, vacation, health offerings, and more.
• A Great Place to Work: Our modern office is designed to foster collaboration and creativity. We provide healthy lunches, snacks, and great coffee to keep you fuelled throughout the day.

Application and information

For more information, please contact Novo Nordisk Foundation Cellerator Head of Quality Johan Söderqvist, , Apply as soon as possible, but no later than 07 November 2025.

To apply, please send your CV, cover letter, and university transcripts, as well as upper secondary school by clicking on the "Apply now" button.

We look forward to welcoming you to Novo Nordisk Foundation Cellerator

About Novo Nordisk Foundation Cellerator

Novo Nordisk Foundation Cellerator is a pioneering initiative dedicated to accelerating the development and manufacturing of cell-based therapies. Located in Lyngby, Denmark, our state-of-the-art facility is designed to bridge the gap between laboratory breakthroughs and clinical application, enabling transformative treatments for chronic and life-threatening diseases.

Our mission is to empower researchers and innovators by providing GMP-compliant manufacturing, process development, and regulatory support for a wide range of cell therapy types—including those derived from pluripotent and adult stem cells. We serve both academic institutions and industry partners, fostering collaboration across sectors to advance regenerative medicine.

As part of the Novo Nordisk Foundation's strategic commitment to health and sustainability, Cellerator operates as a philanthropic entity with a strong focus on impact and excellence. We are building a dynamic, inclusive, and purpose-driven workplace where curiosity, collaboration, and scientific rigor thrive.

In the coming years, Cellerator will expand its capabilities and team, offering exciting opportunities to be part of a growing organization at the forefront of cell therapy innovation. Join us in shaping the future of medicine—where your work contributes directly to improving lives and advancing science.