Job Description

Manufacturing site - GMP documentation

Are you a motivated Junior Validation Associate (m/f/d) eager to grow in a dynamic GMP-regulated environment and extend your first hands-on experience in validation activities within pharmaceutical manufacturing environment? Our client seeks your motivation and eagerness to push validation projects throughout his manufacturing site in the French speaking part of Switzerland. Starting date is June 2026. This is a contract lasting 8 months.

Your Responsibilities:

• Support validation activities for equipment, processes, and systems
• Assist in the preparation and execution of validation protocols (IQ/OQ/PQ)
• Review and maintain GMP documentation
• Collaborate with cross-functional teams such as Production, Quality Assurance, and Engineering
• Contribute to continuous improvement initiatives

Your Profile:

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Engineering, or a related field
• First practical experience (internships, working student roles) in GMP pharma manufacturing
• Strong GMP documentation skills
• French communication level mandatory, good English
• Eagerness to learn and grow in a regulated industry
• Structured, detail-oriented working style

What our client offers:

• Hands-on training in validation and GMP processes
• Mentorship from experienced professionals
• Career development opportunities in Quality and Validation
• A collaborative and supportive team environment