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:
- Bachelors or Masters 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
Manufacturing site - GMP documentationAre 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 e...
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:
- Bachelors or Masters 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
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