Engineer CSV Pharma

French speaking Switzerland - final dosage forms

Are you a tech-savvy engineer eager to apply your knowledge in real-world pharma manufacturing environments? Do you speak French and have a strong grasp of IT systems? This is your opportunity to join a forward-thinking team working on exciting validation projects in the French speaking part of Switzerland – with a 2-year contract in sight.

What You’ll Do
As a CSV & Validation Engineer, you’ll play a key role in qualifying and validating cutting-edge equipment and systems that support the production of life-saving medicines. You’ll work hands-on across labs, warehouses, utilities, and manufacturing lines, helping ensure regulatory compliance and data integrity every step of the way.

Your Impact

• Develop and execute CSV strategies for complex systems like MES, ERP, LIMS, and more
• Lead risk assessments and validation activities across the site
• Interface with external vendors and internal teams to drive key deliverables
• Author and review validation documentation (protocols, reports, traceability, etc.)
• Support audits and continuous improvement efforts with autonomy and confidence

Why This Role?

• Real Project Work from Day 1 through 2027
• Strong On-Site Presence (80–100%) – Be where the action happens
• A Career Foundation – Build future-proof skills in pharma tech & compliance
• Collaborative Environment – Work closely with engineers, technicians & global teams
• French + English – A truly bilingual experience

What You Bring

• Degree in Engineering, IT or a related field
• 5+ years of experience in CSV (Computer System Validation)
• Solid grasp of cGMP, GAMP, 21 CFR Part 11, EU GMP, Annex 11
• Strong knowledge of MES and interfacing systems
• French language skills are mandatory
• Knowledge of oral solid dosage manufacturing is a plus

Interested in shaping the future of pharma operations? Apply now to be one of three engineers joining the CSV team at our customer!