CQV Engineer (m/f/d)

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.

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Facts about the job

Country
Switzerland
Location
Wallis
Contract type
Contracting
Job-ID
BD8W20&origin=51001
Company
Coopers Group AG