• An internationally operating, innovative Swiss pharmaceutical company, a leader in its field
• Flexible working hours and extensive training opportunities
• A motivated multicultural team and environment

• Batch release of clinical supplies (packaged and labeled finished goods, materials, and components), including review and approval of GMP documentation and issuance of batch certificates.
• Deviation, and incident management: evaluation, QA oversight, support to investigations, and approval of records.
• Change control management for GCS processes and documentation.
• Write, review, and approve GMP-relevant documents (SOPs, CoAs, risk assessments, checklists, packaging & labeling documentation).
• Support audits and inspections for TRD GCS topics.
• Provide QA support for GCS operations and ensure alignment with TRD QA standards.

• Master’s degree in life sciences or equivalent education.
• 3–5 years of Pharma QA experience, ideally in development, manufacturing, packaging, or clinical supply.
• Strong knowledge of cGMP and QA processes (batch release, deviations, changes).
• Hands-on experience with SAP (materials management, batch records, release workflows).
• Experience with 1QEM is a strong asset.
• Excellent communication and decision‑making skills.
• Fluent German and English (oral & written).

Nice to have:

• Experience in packaging and labeling operations or in global clinical supply chains.
• Experience collaborating with CMOs or external partners.

Fragen?