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: hugo.palejowski@swisslinx.com .
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