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16395en
- Contract
- English
- Associate
- 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 Specialist. 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: ASAP
Location: Visp, Canton Wallis
Workload: 100%
Duration: 7 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 CAPA’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.
• Bachelor’s Degree in Science or Technical field.
• Business fluent English, German is an advantage.
What's on offer
• An initially 7-month contract.
• A great opportunity to develop your career at a leading international biotechnology company.
If this sounds like you, don’t hesitate to apply here or reach out directly to Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com.
Contract type: Contract
Start Date: ASAP
Location: Visp, Canton Wallis
Workload: 100%
Duration: 7 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 CAPA’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.
• Bachelor’s Degree in Science or Technical field.
• Business fluent English, German is an advantage.
What's on offer
• An initially 7-month contract.
• A great opportunity to develop your career at a leading international biotechnology company.
If this sounds like you, don’t hesitate to apply here or reach out directly to Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com.
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