Job Title: QA Specialist / Batch Record Review
Client: Real Staffing
Location: Valais, Switzerland
Job Category: Other
Job Reference: 30e702e6f56d
Job Views: 4
Posted: 28.04.2025
Expiry Date: 12.06.2025
Job Description:
Responsibilities:
Review electronic and manufacturing protocols for GMP compliance and support protocol revisions.
Ensure adherence to GMP standards and regulatory requirements.
Participate in investigations to assess product quality impacts and define corrective actions.
Represent the Quality Unit in cross-functional teams and make independent quality decisions.
Review and approve validation documents.
Requirements:
Degree in Biology, Chemistry, Biotechnology, Life Science, or related field, or relevant industry experience.
Experience in GMP-regulated pharmaceutical industry is preferred.
Fluency in English; German language skills are advantageous.
Ability to prioritize tasks and meet project deadlines in a fast-paced environment.
Excellent communication skills.
Please send your CV and expected hourly rate if interested. Note: Applicants must have a European passport or Swiss work permit/citizenship due to location constraints.
Sthree Switzerland is acting as an Employment Business for this vacancy.
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