Pharmaceutical Quality Assurance Manager

Vor 5 Tagen


Visp, Schweiz TN Switzerland Vollzeit
Role Overview
Spearhead quality initiatives to ensure compliance with regulatory requirements and industry standards in raw material management. Develop and implement quality control processes to maintain product integrity throughout the manufacturing process.

About the Position
Leverage your expertise in GMP regulations and quality assurance to support strategic growth in Visp. Collaborate with interdisciplinary teams to ensure raw materials meet quality standards, from procurement to release.

Key Responsibilities
  • Maintain quality requirements for raw materials in a GMP environment.
  • Review and approve raw material-specific documents (QC plans, sampling instructions, material lists, etc.).
  • Support OOS investigations, deviations, CAPAs, and change control processes.
  • Participate in regulatory inspections and audits as subject matter expert.

Requirements
(B.Sc.) in Chemistry, Biology, Biochemistry, Biotechnology, or comparable qualification required. Experience in the GMP environment and manufacture of 'Drug Products' is an advantage. Fluent German and English skills are essential.

About Our Culture
We prioritize ethics and respect for our people and environment. Our mission is to improve lives worldwide through life sciences solutions. Join us to drive meaningful impact.

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