Sr Engineer in CQ and CSV Pharma
Sr Engineer in CQ and CSV Pharma
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1 Vacancy
Job Description
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 Youll 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 EUGMP 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
- youll 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.
Employment Type
Full Time
