Contract QA Validation Lead, GMP & Biotech Manufacturing

CTC Resourcing Solutions

Wallis

Vor Ort

CHF 120.000 - 150.000

Vollzeit

Vor 8 Tagen

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Zusammenfassung

The Life Science Career Network seeks a QA Validation Manager for a contract position in the Valais region of Switzerland. You will ensure critical GMP processes are validated and maintained to meet product requirements, process parameters, and global regulatory guidelines.

You will collaborate with MSAT, Manufacturing, and clients to provide scientifically sound, documented evidence and oversee CPV and validation activities, while supporting audits and continuous improvement initiatives.

Qualifikationen

  • Bachelor's degree in Science, Biotechnology, or related field.
  • 5–7 years of pharma GMP experience.
  • Strong knowledge of process and cleaning validation.
  • Experience with change controls and deviation management.
  • Knowledge of cell/gene manufacturing is a plus.
  • English proficiency; German is a plus.

Aufgaben

  • Validate and maintain GMP processes per product requirements and global guidelines.
  • Collaborate with MSAT, Manufacturing, and clients to provide validated, documented evidence.
  • Oversee validation activities for biotechnological manufacturing processes in a low bioburden environment.
  • Support cleaning and sanitization validation activities.

Kenntnisse

GMP knowledge
Process validation
Cleaning validation
Equipment qualification
Change controls
Deviation management
Non-conformity investigations
Data integrity
English proficiency

Ausbildung

Bachelor's degree in Science/ Biotechnology or related field

Jobbeschreibung

The Life Science Career Network seeks a QA Validation Manager for a contract position in the Valais region of Switzerland. You will ensure critical GMP processes are validated and maintained to meet product requirements, process parameters, and global regulatory guidelines.

You will collaborate with MSAT, Manufacturing, and clients to provide scientifically sound, documented evidence and oversee CPV and validation activities, while supporting audits and continuous improvement initiatives.

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