On behalf of our client, a leading international biotechnology company based in Visp, Swisslinx is looking for a CQV Engineer. In this role, you will lead validation activities across equipment, facilities, and systems, ensuring seamless installation, compliance, and process efficiency, while driving cross-departmental collaboration and maintaining high standards in documentation and quality systems.
Contract type - Contract
Start Date - ASAP
Location - Visp
Workload - 100%
Duration - 6 months with possible extension
Your mission :
- Lead and execute the validation of equipment, facilities, and systems, ensuring compliance with cGMP standards.
- Coordinate equipment installations, and draft and execute IQ / OQ / PQ protocols while documenting results.
- Develop and maintain comprehensive validation documentation, including URS, DQ, FMEA, Risk Assessments, FAT, and SAT.
- Oversee validation activities across the entire lifecycle, conducting GAP analysis, risk assessments, and identifying process efficiencies.
- Manage quality systems activities, including document management, change control, non-conformities, and CAPAs.
- Support the Engineering team in preparing for validation, requalification, and maintenance programs, while staying informed of regulatory changes.
Your background :
Bachelor's degree in Science or a Technical field.5-10 years of advanced-level experience in the pharmaceutical industry, focusing on validation processes.Excellent technical writing skills with attention to thorough, accurate, and timely documentation.Strong written and oral communication skills for effective cross-departmental collaboration.Outstanding organizational and time-management abilities to efficiently manage multiple validation tasks.What's on offer
A 6 month contract.A great opportunity to develop your career at a leading international biotechnology company.A competitive salary.If this sounds like you, don't hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter : [email protected].