Cleaning Validation Specialist; GMP​/MedTech

📍 Central Switzerland | Med Tech (regulated manufacturing) | Hybrid (mainly on-site)

For a modern production site in a highly regulated Med Tech environment, we are looking for an experienced professional in Cleaning Validation and Contamination Control
.

This role sits within a specialized Quality Control context and combines technical depth, GMP expertise and structured documentation work
.

• Plan and execute cleaning validation activities end-to-end
• Develop validation documentation such as master plans, study designs, risk assessments, protocols and reports (incl. IQ/OQ/PQ where applicable)
• Assess and manage changes and deviations impacting cleaning processes
• Contribute to cross‑functional project teams and coordinate validation‑related activities
• Work closely with Production, Engineering and QC stakeholders
• Support the development and implementation of contamination control strategies (depending on experience)

• University degree in a scientific/technical discipline (e.g., Chemistry, Pharmacy, Microbiology, Chemical/Process Engineering or similar)
• Several years of hands‑on experience in cleaning validation within a regulated manufacturing environment
• Solid knowledge of GMP; ISO 13485 is a strong plus
• Strong technical understanding of production equipment and manufacturing processes
• Fluent German and English (documentation and stakeholder communication)

This position requires regular presence on‑site due to interaction with equipment and validation execution.

• A highly specialized expert role with ownership and visibility
• A balanced mix of on‑site execution, project work and documentation
• Collaboration within a focused QC setup and cross‑functional teams
• Attractive employment conditions and development opportunities

• Base salary range:
  CHF 120k–130k (depending on experience)