Sigma
Plan-les-Ouates
Qualification and Validation Technician
- 13 August 2026
- 100%
- Permanent position
About the job
Your mission:
- Writing qualification protocols and reports
- Execution and documentation of qualification and metrology activities (initial and periodic)
- Coordination and control of the various qualification stages with the relevant departments
- Writing and execution of computerised system qualification protocols (URS, IQ, OQ, PQ)
- Control of regulatory compliance of systems according to GMP requirements, 21 CFR Part 11 and Annex 11
- Analysis of discrepancies, documentation of deviations and proposal of corrective and preventive actions (CAPA)
- Participation in the validation of cleaning of production equipment in accordance with current regulations
Your profile:
What we offer:
Individual support for optimising your CV and interview preparation.
Opportunity within a renowned pharmaceutical company.
Temporary assignment with possibility of extension depending on company needs.
Interested?
Please do not hesitate to send us your complete application following the instructions below.
Only applications matching our requirements will be processed
- Degree in qualification/validation, automation or equivalent fields
- Proven experience in qualification/validation of systems and processes in a GMP environment
- Essential experience in the pharmaceutical industry
- Good knowledge of GMP as well as 21 CFR Part 11 requirements
- Experience in CSV (Computer System Validation)
- Fluency in French and English
- Autonomy, rigour, team spirit, sense of responsibility and proactivity
What we offer:
Individual support for optimising your CV and interview preparation.
Opportunity within a renowned pharmaceutical company.
Temporary assignment with possibility of extension depending on company needs.
Interested?
Please do not hesitate to send us your complete application following the instructions below.
Only applications matching our requirements will be processed
