CQV Engineer
On behalf of our client, a leading international biotechnology company based in Visp, Swisslinx is looking for a CQV Engineer. If this is you, you will carry out a variety of tasks related to the validation of equipment and facilities. The scope of activities includes the coordination on the installation of equipment, drafting the IQ/OQ/PQ protocols, execution of the IQ/OQ/PQ and documenting the results according cGMP requirements.
Contract type - Contract
Start Date - September
Location - Visp, Canton Wallis
Workload - 100%
Duration - 6 months
Your mission:
- Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
- The validation documentation deliverables include URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ).
- Prepare validation documents.
- Execution of IQ/OQ and PQ for equipment, systems and utilities.
- Write reports of completed validation activities.
- Work to identify efficiencies in the validation program approach.
- Work to 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 CAPAâ??s.
- Writing and/or revising procedures applicable to the Engineering activities.
- Support the Engineering group to prepare the validation, requalification, and maintenance program.
- Perform other duties as assigned.
Your background:
- 3-6 years of experience in a similar role.
- Bachelorâ??s Degree in Science or Technical field.
- Business fluent English, German is an advantage.
What's on offer
- An initially 6 month contract.
- A great opportunity to develop your career at a leading international biotechnology company.
If this sounds like you, donâ??t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: Write an email.
Contract type - Contract
Start Date - September
Location - Visp, Canton Wallis
Workload - 100%
Duration - 6 months
Your mission:
- Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
- The validation documentation deliverables include URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ).
- Prepare validation documents.
- Execution of IQ/OQ and PQ for equipment, systems and utilities.
- Write reports of completed validation activities.
- Work to identify efficiencies in the validation program approach.
- Work to 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 CAPAâ??s.
- Writing and/or revising procedures applicable to the Engineering activities.
- Support the Engineering group to prepare the validation, requalification, and maintenance program.
- Perform other duties as assigned.
Your background:
- 3-6 years of experience in a similar role.
- Bachelorâ??s Degree in Science or Technical field.
- Business fluent English, German is an advantage.
What's on offer
- An initially 6 month contract.
- A great opportunity to develop your career at a leading international biotechnology company.
If this sounds like you, donâ??t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: Write an email.
About the company
