Pharmaceutical Process Engineer

3 days ago


Hillerød, Hillerød Kommune, Denmark Novo Nordisk AS Full time
Job Description

We are seeking a skilled Pharmaceutical Process Engineer - Regulatory Compliance Specialist to join our team at Novo Nordisk A/S. As a key player in the Validation Support team within the Project Quality Management (PQM) department, you will be responsible for ensuring that validation structures and processes are robust and effective.

In this role, you will:

  1. Guide and support work package owners (WPOs) with commissioning, qualification, and validation (CQV) activities to ensure compliance with the prescribed validation approach (GMP and GEP).
  2. Maintain a strategic overview of validation structures and processes to identify areas for improvement and implement changes as needed.
  3. Collaborate with various stakeholders to facilitate seamless execution of CQV activities and meet project objectives.

To excel in this role, you should have:

Qualification Requirements
  1. A scientific academic degree in engineering, biology, chemistry, pharmacy, or a related field.
  2. At least 2 years of experience in working with validation, having previously held roles as both Engineering Responsible (ER) and Operation Responsible (OR).
  3. Experience in API production.
  4. Full proficiency in spoken and written English.

About Us

Novo Nordisk A/S is one of the world's leading healthcare companies, and we're committed to driving change to defeat serious chronic diseases. Our vision is to lead the way in shaping a healthier future for people worldwide.



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