I am on the search for a QA Specialist to join an established Medical Device and Pharmaceutical leader based in Copenhagen.

You will be take accountability of being the Quality Responsible Person and collaborate closely with other Nordic QA/Responsible Persons to maintain ongoing QA/GDP compliance within Denmark.

You will be responsible for:

• Implement and maintain a quality management systems
• Ensure full compliance with national QA and GDP requirements and processes
• Decide on the final disposition of returned, rejected, recalled, or falsified products
• Handle complaints, counterfeits, and product defects as required
• Collaborate with other Nordic/UKI and Global RA leads to handle and implement regulatory strategies
• Ensure regulatory compliance for medicinal products and medical devices

You will bring the following:

• Strong GMP and GDP knowledge within Pharmaceuticals and Medical Device
• Fluent in English and Danish
• A degree in Life Science or equivalent