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:
- Responsible for ensuring compliance with GMP and regulatory requirements
- Conduct regular audits of data, equipment, and systems
- Review and approve production and analytical documentation
- 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.