GMP Auditor

5 dni temu


Łódź, Łódź Voivodeship, Polska CK Group- Science, Clinical and Technical Pełny etat

Join us as a GMP Auditor at our biopharmaceutical client's site in London.

About the role:

  1. Responsible for ensuring compliance with GMP and regulatory requirements
  2. Conduct regular audits of data, equipment, and systems
  3. Review and approve production and analytical documentation
  4. Participate in training and development programs to maintain knowledge of regulations and best practices

We're looking for someone with:

  • A degree in a relevant scientific field or equivalent experience
  • Previous experience in a quality function, preferably within the pharmaceutical or chemical industries
  • Excellent communication and analytical skills
  • Ability to work independently and as part of a team

This is a great opportunity to develop your career as a quality professional in a dynamic industry.