QA Manager; m​/w​/d

We are offering a unique opportunity to join our client on a temporary assignment within the Synthetic Molecules IMP group in Basel as a QA Manager (m/w/d). This role gives you the chance to take ownership of quality excellence within Drug Manufacturing Operations at the Basel site, collaborate closely with experienced interdisciplinary teams, and actively contribute to shaping the future of IMP manufacturing activities.

We offer a 12‑month temporary contract with the option for extension in Basel.

The mission of the Synthetic Molecules IMP Quality group includes providing quality oversight for the Synthetic Molecules Drug Substance and Drug Product operations, as well as the associated quality control activities.

The ideal candidate holds a Master’s degree in a scientific discipline and brings more than 10 years of professional experience in the pharmaceutical industry, including at least 5 years in Quality Assurance. A solid understanding of cGMP and quality requirements for clinical development phases, as well as a proven track record in inspections, is required. The candidate also brings strong computer skills and fluency in German and English.

• Review of Drug Product Batch Records in collaboration with the relevant departments
• Execution of IMP Drug Product release
• Review and approval of documents, such as specifications, risk assessments, deviation reports, and change control records
• Review and approval of cleaning protocols and cleaning reports
• Support for assigned departments regarding GMP‑related questions
• Conducting self‑inspections

• Completed Master degree in scientific field
• At least 10 years of professional experience in the pharmaceutical industry, including at least 5 years in Quality Assurance
• Knowledge of cGMP and quality requirements for clinical development phases
• Proven success in health authority inspections and internal GMP audits
• Good IT skills (MS Office) – especially experience with SAP and other quality management systems (e.g., Veeva Vault)
• Fluent in English and German, both written and spoken

• Professional experience in pharmaceutical development (Synthetic Molecules Drug Product)
• Additional Information:
• Latest possible start date: 01.03.2026 / 15.03.2026
• Planned duration of employment: 12 months
• Extension: high probability
• Work location:
  
  Basel
• Workload: 100%
• Home office:
  On-site required, max 20%
• Team size: 10 people

Are you looking for a new challenge? Do not hesitate and APPLY NOW!