MSAT Cleaning Validation Expert  

Your Responsibilities

• Lead and execute equipment cleaning validation activities (CIP, COP, USP, DSP, buffer/media systems)
• Author and review validation protocols, reports, and GMP SOPs
• Support execution of cleaning validation, including parts washer (COP) validation
• Ensure compliant implementation of validated cleaning processes in manufacturing
• Coordinate cross-functional activities with MSAT, QA, QC, Manufacturing, and R&D
• Perform impact assessments for deviations, changes, and technical change requests (DRs, CRs, TCRs)
• Act as a technical subject matter expert in cleaning validation projects
• Support customer and regulatory inspections (FDA, EMA)
• Contribute to continuous improvement and standardization of cleaning validation practices

Your Profile

• Degree in Life Sciences, Biotechnology, Chemical Engineering, or related field
• Proven experience in GMP cleaning validation within pharmaceutical or biopharmaceutical manufacturing
• Hands-on experience with equipment cleaning validation (CIP, COP, USP, DSP)
• Strong knowledge of regulatory requirements (FDA, EMA)
• Experience with deviation and change management processes
• Excellent documentation and data analysis skills
• Strong communication and collaboration abilities
• Fluent in English (German is an advantage)

Additional Information

• Location: Visp, Switzerland
• Workload: 100% (on-site)
• Start: ASAP
• Duration: Until December 31st, 2026 (extension possible)

Interested?

We look forward to receiving your application. Please submit your CV in English.