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16376en
- Contract
- English
- Mid-Senior level
- Engineering & Technical Services
- Switzerland
- Healthcare & Life Sciences
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.
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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