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15984en
- Contract
- English, German
- Mid-Senior level
- Engineering & Technical Services
- Switzerland
- Healthcare & Life Sciences
Skills
CQV engineer, validation, IQ/OQ, PQ, industry regulatory, Quality Systems activities, technical writing
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This vacancy has now expired
On behalf of our client, a leading international biotechnology company based in Visp, Swisslinx is looking for a Commissioning Qualificaion Validation engineer (CQV engineer). If this is you, you will be responsible for the validation of equipment and facilities at the company's site.
Start Date: ASAP
Location: Visp
Workload: 100%
Work type: 100% on site
Duration: until end of 2024
Your mission:
• Support all validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
• Prepare validation documents.
• Execution of IQ/OQ and PQ for equipment, systems and utilities.
• Write reports of completed validation activities.
• Identify efficiencies in the validation program approach.
• Apply lessons learned and stay informed of industry regulatory changes as it applies to equipment / facility validation.
• Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA’s.
• Write and/or revise procedures applicable to the Engineering activities.
• Support the Engineering group to prepare the validation, requalification, and maintenance program.
Your background:
• German mandatory (English a real plus)
• 5+ years experience in the pharma industry
• Bachelor’s Degree in Science or Technical field.
• Excellent technical writing skills and the ability to document all work in a thorough, accurate and timely manner.
• Excellent written and oral communication skills and the ability to work interdepartmentally in an effective manner to carry out daily duties.
• Excellent organizational and time management skills.
What's on offer:
• a 10 month contract, with possibility of extension
• a great opportunity to develop your career at a leading international biotechnology company
If this sounds like you, apply down below or reach out directly to Hugo Palejowski, recruiter: hugo.palejowski@swisslinx.com
Start Date: ASAP
Location: Visp
Workload: 100%
Work type: 100% on site
Duration: until end of 2024
Your mission:
• Support all validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
• Prepare validation documents.
• Execution of IQ/OQ and PQ for equipment, systems and utilities.
• Write reports of completed validation activities.
• Identify efficiencies in the validation program approach.
• Apply lessons learned and stay informed of industry regulatory changes as it applies to equipment / facility validation.
• Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA’s.
• Write and/or revise procedures applicable to the Engineering activities.
• Support the Engineering group to prepare the validation, requalification, and maintenance program.
Your background:
• German mandatory (English a real plus)
• 5+ years experience in the pharma industry
• Bachelor’s Degree in Science or Technical field.
• Excellent technical writing skills and the ability to document all work in a thorough, accurate and timely manner.
• Excellent written and oral communication skills and the ability to work interdepartmentally in an effective manner to carry out daily duties.
• Excellent organizational and time management skills.
What's on offer:
• a 10 month contract, with possibility of extension
• a great opportunity to develop your career at a leading international biotechnology company
If this sounds like you, apply down below or reach out directly to Hugo Palejowski, recruiter: hugo.palejowski@swisslinx.com
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