In this role, you are supporting the release and stability strategy, the method validation and method transfer activities for our products covering development activities. You will support the operational aspects of GMP testing of Biologics clinical drug substances (DS) and drug products (DP). You independently manage your activities and provide required documentation according to agreed timelines and standards. Further, you will review high-quality CMC documentation for HA submission.
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Global Pharma Company.
If you are interested then kindly send your resume to: firstname.lastname@example.org
- Quality Control experience in a GMP environment and/or pharmaceutical industry experience desired - Sound technical and scientific knowledge of pharmaceutical development and analytical sciences desired - Knowledge on health authority regulations is a plus - Proven ability to critically evaluate data from a broad range of scientific disciplines
Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology)
English : Very good