In this role, you are ensuring that all process and product related activities in the area of Quality Control are following legal requirements, GMP guidelines and relevant policies of our client.

Tasks and responsibilities

• QA release of excipients and other direct materials
• Evaluation and assessment of change records
• Review and approval of relevant GMP-documents
• OOS, deviation management and CAPA review and approval
• Review and approval of risk assessments in the area of responsibility
• Collaboration with our interfaces to Quality Control (QC) personnel and other departments to ensure a constant state of inspection readiness by identifying, escalating and working to resolve compliance risks in the area

Main requirements 

• Master degree or PhD in Life Sciences and preferably 5 years of relevant experience in the pharmaceutical industry in a similar role
• Demonstrated experience in quality assurance (and additionally preferably quality control)
• Knowledge of cGMP and quality requirements
• Results-oriented, analytical working style
• Agile mindset, that is characterized by embracing change and the ability to work in self-organizing teams
• Ability to communicate clearly and professionally both verbally and in writing in German (C2) as well as English (C1)

General information

• Start date: asap (latest end of February)
• Planned duration: 6 months
• Workplace: Basel
• Workload: 100% (mostly onsite)

 If you are interested in this position, please send your CV in German.