Analytical QC Compliance Specialist (12-month contract)

About the role

The company, a leading global player in drug discovery and personalised healthcare, is seeking an Analytical QC Compliance Specialist for a 12‑month contract in Basel. The role supports the quality control department in maintaining cGMP compliance and managing compliance records.

Key responsibilities

• Manage compliance records including deviations, change controls and CAPAs.
• Coordinate with QA, scientists and senior management to ensure proper documentation and stakeholder alignment.
• Facilitate root‑cause analyses and document findings.
• Participate in quality review boards and other governance bodies.
• Provide inspection support, preparing and presenting records to internal and external auditors.
• Critically evaluate own work results and uphold GMP standards.

Required profile

• Master’s degree (or higher) in Organic Chemistry, Analytical Chemistry, Pharmacy or related natural science.
• 3‑5 years of experience in a regulated pharmaceutical or biotech environment.
• Hands‑on experience with cGMP regulations.
• Residency permit or Swiss/EU citizenship.
• Fluent written and spoken English; German is a strong asset.

Required skills

• Proficiency with a Quality Management System such as Veeva Vault or TrackWise.
• Strong knowledge of cGMP compliance processes.