Validation Engineer – Pharmaceutical Equipment
Clean-in-place and sterilization systems
For our client, a leading pharmaceutical company based in Switzerland, we are looking for a
Validation Engineer – Pharmaceutical Equipment 100% (Ref. Nr. 3015)
Clean-in-place and sterilization systems
Your main tasks
Plan and execute IQ, OQ, and PQ validation protocols for pharmaceutical equipment.
Validate CIP/SIP systems, autoclaves, and fill-finish equipment.
Prepare validation master plans, protocols, and summary reports.
Support computer system validation (CSV) activities per GAMP 5 guidelines.
Manage change controls and revalidation activities.
Your profile
Degree in Engineering, Pharmaceutical Sciences, or related technical field.
3-5 years of validation experience in pharmaceutical manufacturing.
Knowledge of EU GMP Annex 15, FDA process validation guidance, and ISPE guidelines.
Experience with GAMP 5 and computerized system validation.
Strong documentation skills and attention to regulatory detail.
