Senior Qualifying Specialist

Location: Switzerland (100% on-site)
Contract type: Full-time
Language: German (mandatory); English a strong plus

Join a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.

• Plan and coordinate CQV for facilities & utilities (e.g., HVAC, clean/black utilities) and production equipment.

• Author, review, execute and report IQ/IOQ/OQ/PQ protocols and related documentation.

• Produce and maintain validation deliverables: URS, DQ, FMEA, Risk Assessments, FAT, SAT, and final reports.

• Drive gap analyses and continuous improvement across the validation lifecycle; apply lessons learned and regulatory updates.

• Perform Quality Systems ...