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Regulatory Affairs Specialist

Want to drive compliance across global markets and contribute to a mission of improving healthcare access worldwide?

Join us as a Regulatory Affairs Specialist in our new office in Copenhagen and play a key role in ensuring our medical devices meet regulatory requirements in over 85 markets.

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FOSS

Wine & Meat R&D Director

Hillerød

For FOSS’ R&D management team, we are seeking a new R&D Director for our Wine & Meat business unit. The unit is responsible for turnover, growth, profitability, and bringing new innovative analytical solutions to the market within Wine & Meat.

As R&D Program Director, you will work across the organization, bridging R&D, Sales & Marketing, and Service within the business unit.

FOSS
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Clinical Trial Administrator - Maternity cover

København S

Are you passionate about making a difference in the field of clinical trials?

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Advanced QA Professional

Hillerød

Are you passionate about ensuring quality in pharmaceutical production?

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Analytical Project Manager Drug Substance

Taastrup

Do you want to join us on our journey unfolding an ambitious strategy for chemical synthesized APIs (Active Pharmaceutical Ingredients).

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CMC Submission Specialist

Høje Taastrup

Are you interested in being a key contributor within Chemistry, Manufacturing & Control (CMC) in the process of preparing successful drug registrations for Novo Nordisk?

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GMP Material Professional

Køge

Do you have a sharp eye for detail and a strong understanding of GMP documentation?

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Manager/Senior Manager, CMC API Downstream Development

Bagsværd

Ready to join a business area that ensures the success and development of robust Active Pharmaceutical Ingredients (API) processes for the...

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Outsourced Production Scientist - Aseptic Clinical Trials

Måløv

Are you ready to be part of a dynamic team collaborating with internal stakeholders in project teams and Contract Manufacturing Organisations (CMO) worldwide?

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Regulatory Writer

Bagsværd

Are you passionate about understanding the needs of medicines authorities and re-writing our internal documentation into regulatory submissions?

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Director, Real World Evidence (RWE)

København S

Ready to shape the future of healthcare with real-world data across Europe & Canada?

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Manager in Customer Complaint Operations Denmark - Join us in making a difference for patients

Bagsværd

Are you passionate about leadership and inspiring others?

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Senior Filling/Formulation Scientist

Søborg

Could you be looking for an opportunity to play a key role in developing new injectable drug products to treat serious chronic diseases?

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Aseptic Manufacturing Specialist

Bagsværd

Do you have expertise within Aseptic Manufacturing and perhaps Formulation in particular and looking to challenge yourself in a high-paced filling factory?

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Aseptic Production Supporter

Kalundborg

Are you motivated by the pulse of a Good Manufacturing Practice (GMP) production area?

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Senior QA professional for QC - Emerging Technologies Quality

Måløv

Are you passionate about setting direction within emerging technologies and ensuring compliance?

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Senior Regulatory Professional for Rare Bleeding Disorders area (maternity cover)

Søborg

Are you able to cut through complexity and drive regulatory strategies for high impact projects?

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Manager in Global QC Raw Materials

Hillerød

We´re seeking a Manager to lead one of three teams in the Global QC Raw Materials organization.

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Corporate Vice President for Metabolic and Cardiovascular Therapy Areas in Global Medical Affairs

Søborg

We are looking for a senior executive ready to join the journey in transforming Global Medical Affairs in Novo Nordisk and drive impact to improve patient outcomes.

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Senior Global Trial Manager

Søborg

Do you possess the expertise to drive clinical trial progress within an international HQ team?

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