Senior QA Projects Manager – Western Switzerland

BioTalent is currently supporting a leading global pharmaceutical CDMO organisation that are seeking a highly motivated and experienced Senior QA Projects Manager. You will act within the site's key projects teams as the main Quality Operations representative and single point of contact for QA, QC, Compliance and Quality Suppliers.

Key Responsibilities:

• Compliance & Projects: Support regulatory compliance and represent Quality in key projects.
• Quality Coordination: Manage quality for tech transfer, supplier qualification, and manufacturing; liaise with customers.
• Regulatory Support: Handle change control and regulatory inquiries.
• Quality & Safety: Ensure site Quality and safety compliance.

Requirements:

• Extensive QA, QC, and RA experience in the pharmaceutical industry.
• Expertise in cGMPs and regulatory compliance for Swiss, EU, and FDA standards.
• Proven track record across all phases of drug development, from clinical trials to product launch.
• Specialized knowledge in oral solid dosage manufacturing, packaging, testing, warehousing, validation, and registration.
• Strong strategic leadership with the ability to align business strategy with practical execution.

This is an excellent opportunity to get involved as a global leader whilst working at the forefront of science with a strong culture of collaboration.

Please apply / email your resume with a convenient time to Duncan.johnston@biotalent.com to have a confidential discussion about this opportunity.