Quality Assurance Specialist

2 weeks ago


Copenhagen, Copenhagen, Denmark Lundbeck Full time

Unlock Your Potential in Pharmaceutical Quality Assurance

Lundbeck is seeking a highly skilled and motivated Quality Assurance Specialist to join our CMC Development QA team. As a key member of our team, you will play a critical role in ensuring the quality and compliance of our investigational medicinal products (IMPs) for clinical trials.

About the Role

You will be responsible for reviewing batch records, conducting QA assessments of deviations, change controls, and laboratory deviations, and approving master batch records. Additionally, you will handle complaints and contribute to vendor oversight, including vendor re-evaluations.

What We Offer

We offer a dynamic and collaborative work environment, with opportunities for growth and development. You will work closely with multiple stakeholders in CMC and contribute to the continued development of our processes.

Requirements

  • Master's degree in pharmacy, chemistry, biology, or a related field
  • Minimum 2 years of experience in a GMP regulated environment, preferably in manufacturing, quality control, or quality assurance
  • Knowledge and competencies within CMC are preferred
  • Fluency in English

Why Lundbeck?

We are committed to building a diverse and inclusive workforce, and we believe that every brain in the game is essential to our success. We offer a range of benefits, including opportunities for professional development, a collaborative work environment, and a commitment to work-life balance.

Apply Now

If you are a motivated and experienced Quality Assurance Specialist looking for a new challenge, we encourage you to apply. Please upload your CV and include a few lines about your motivation for applying. We look forward to hearing from you



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