GMP Bioprocess Engineer – Batch Records & Deviations

Barrington James; Genf; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

Barrington James is seeking a Bioprocess Engineer for an 8-month on-site contract in Visp, Switzerland. The role focuses on reviewing and clearing a backlog of executed batch records and related GMP documentation, while supporting deviations, CAPAs, and change controls within a GMP framework.

Ideal candidates will have 3–4+ years in biopharma, German-language batch review experience, and Downstream Processing exposure, with hands-on DP and compliance activities.

Qualifikationen

• 3–4+ years in biopharma manufacturing or bioprocessing.
• Experience reviewing batch records in GMP.
• Fluent German; must review German batch docs.
• Experience with DP, CAPA, and change control.
• Aseptic fill-finish experience is desirable.

Aufgaben

• Review and clear executed batch records and GMP docs.
• Backlog clearance during first three months.
• Identify discrepancies and address missing information.
• Support deviations and CAPAs, heavy on documentation.
• Assist DP manufacturing and process activities.
• Coordinate change controls in GMP environments.
• Support autoclave and washing processes.
• Collaborate with manufacturing, QA and cross-functional teams.
• Ensure GMP compliance across activities.

Kenntnisse

GMP documentation

Batch records review

Deviation management

CAPA & change control

Downstream Processing

Autoclave processes

Cross-functional collaboration

Documentation discipline

Jobbeschreibung

Barrington James is seeking a Bioprocess Engineer for an 8-month on-site contract in Visp, Switzerland. The role focuses on reviewing and clearing a backlog of executed batch records and related GMP documentation, while supporting deviations, CAPAs, and change controls within a GMP framework.

Ideal candidates will have 3–4+ years in biopharma, German-language batch review experience, and Downstream Processing exposure, with hands-on DP and compliance activities.