Validation Engineer

7 days ago


Hillerød, Hillerød Kommune, Denmark Novo Nordisk AS Full time

We are seeking an experienced Validation Engineer to join our team at Novo Nordisk A/S. As a key member of our Global Contract Manufacturing Devices department, you will play a critical role in introducing new production equipment and ensuring compliance with GMP regulations.

About the Role

The successful candidate will be responsible for reviewing validation documentation from our contract manufacturers, collaborating with stakeholders, and owning the supplier validation agreement process. This requires strong analytical skills, attention to detail, and effective communication abilities.

Key Responsibilities

  • Review and validate installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) documents
  • Collaborate with equipment responsibles, QA, project managers, contract manufacturers, and other validation engineers to ensure seamless integration
  • Owning the supplier validation agreement process to ensure compliance and continuous improvement

Requirements

  • Masters degree in life science or engineering
  • Full proficiency in English, written and oral
  • Experience with validation processes, including IQ, OQ, and PQ
  • Familiarity with pharmaceutical/medical device industry regulations

Working Conditions

This is a full-time position based in Hillerød, Denmark. You will work closely with a dedicated team of approximately 70 engineers and professionals who share your passion for delivering high-quality medical devices.

Benefits and Compensation

We offer a competitive salary of DKK 625,000 - 825,000 per year, depending on experience, as well as excellent benefits and opportunities for professional growth and development.

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