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CQV Engineer
m/w/d, Wallis
Are you experienced in validation of equipment and facilities in a pharmaceutical environment? Now you want to leverage your knowledge and work on global projects?
Our client is looking for support in their validation team in Visp.
Start date: Immediately
Duration: 1 year
Responsibilities:
- 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.
- Involved in all validation activities including but not limited to: 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).
- Execution of IQ/OQ and PQ for equipment, systems and utilities.
- Write reports of completed validation activities.
- Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA’s.
Your background:
- Degree in Science or Technical field.
- At least 5 years of experience in pharma Industry in CQV.
- Experience in drafting the IQ/OQ/PQ protocols.
Job Profil
- Wallis
- Contracting
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Jessica Arber
Talent Acquisition Consultant
+41 61 638 38 41
jessica.arber@coopers.ch