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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: