Sr. Engineer in C&Q and CSV Pharma

qualification/validation activities for equipment, systems, and processes

Our client is a leading biopharmaceutical company, renowned for its globally recognized product portfolio. To support a significant ongoing investment project, we are seeking an experienced C&Q Engineer to join their Manufacturing & Technical Services Team

What You’ll Do

• Lead and execute qualification/validation activities for equipment, systems, and processes.
• Develop and implement C&Q and CSV strategies based on risk assessment and scientific rationale.
• Ensure compliance with cGMP standards, local policies, and global strategies.
• Collaborate with internal and external teams, including vendors, to maintain operational excellence.
• Serve as a Subject Matter Expert (SME) in audits, change controls, and risk assessments.

This specific assignment shall be started in March and is planned for 8 months with high probability of prolongation till 2026!

Your Profile

• Experience: 5+ years in pharmaceutical validation.
• Education: BS/MS in Engineering or related technical field.
• Skills: Proficiency in cGxP, 21 CFR Part 11, EU-GMP, GAMP, and data integrity principles.
• Languages: Fluent in English; French is a plus.
• Location: Based in Switzerland or holding a Swiss work permit.

Why Join?

• you’ll be at the forefront of manufacturing excellence and new product introductions in oral solid dosage forms. Join a collaborative environment that fosters innovation and professional growth.