Jobs in Copenhagen
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QARA Consultant
We are seeking a QARA Consultant to support cross-functional teams in the development, manufacturing, and regulatory submission of combination products. Key Responsibilities:Provide regulatory and quality guidance on combination products, particularly those involving drug-device interactions.Support US regulatory specialists in the preparation and ...
Freelance Clinical Research Associate (m/f/d)
Are you an experienced Clinical Research Associate (CRA) seeking a flexible freelance opportunity within the innovative world of medical devices? Do you want to work remotely, managing clinical research studies across the Nordic region while enjoying the freedom of flexible hours and competitive pay?EPM Scientific is proud to be partnering with a l...
Business Development Director
Business Development Director - Drug Discovery CRO (Europe) Location: Europe (Remote or Hybrid with travel) Industry: Drug Discovery & CRO Employment Type: Full-Time Experience Level: Mid to Senior LevelThe organisation is a fast-growing, innovation-driven Contract Research Organisation (CRO) specializing in early-stage drug discovery. Our mission...
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Regulatory Consultant
We are looking for an experienced and detail-oriented Regulatory Affairs Consultant to join our team on-site in Denmark. This role is ideal for someone with a strong background in medical device regulations who thrives in a collaborative, fast-paced environment. You will play a key role in ensuring compliance with EU MDR and other global regulatory...
Quality Assurance Specialist
We are seeking an experienced Quality Assurance Specialist for a 12-month contract. This role will support ongoing GxP compliance efforts across manufacturing, quality systems, and regulatory operations. The ideal candidate will bring a broad background in pharmaceutical QA.Key Responsibilities:Ensure compliance with GxP regulations across operatio...
Quality Engineer Consultant
We are seeking an experienced Quality Engineer to join a client of EPM Scientifics team in the medical device industry. The ideal candidate will have over 5 years of experience in quality engineering, with a strong background in ensuring compliance with regulatory standards and improving product quality. This role involves working closely with cros...