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Tasks:
Maintain and continuously improve hygiene standards at the Visp site
Act as the interface between Production, QA, Monitoring, Engineering, and EHS for contamination control
Lead hygiene projects (gowning, cleaning, disinfection, material transfer, cleanroom behavior)
Plan and execute Cleanroom Performance Qualifications (PQs) in compliance with GMP
Manage GMP documentation related to hygiene processes
Investigate deviations, perform root cause analyses, and manage CAPAs and change requests
Ensure timely handling and closure of deviations within the quality system
Drive standardization and improvement of hygiene processes across production areas
Support audits and inspections, representing hygiene topics
Develop and deliver hygiene training programs
Qualification:
Scientific degree or equivalent (e.g., Chemistry, Pharmacy, Bioprocess Engineering)
Experience in a GMP-regulated environment, ideally in contamination control or quality
Strong knowledge of GMP and related documentation (SOPs, CAPAs, deviations, change controls)
Fluent in English; German is an advantage
Analytical, structured, and solution-oriented approach
Strong communication and teamwork skills
Independent, responsible, and quality-focused mindset
Requirements:
Start: 27.04.2026
Duration: 8 months
Capacity: 5 days per week
Location: Visp