We are actively looking for a CQV Engineer for a pharmaceutical laboratory in Viège.

CQV ENGINEER - Temporary position

Mission :

Ensure the commissioning, qualification and validation of equipment, installations and utilities in a cGMP pharmaceutical environment. Draft and execute the IQ/OQ/PQ protocols and ensure compliant, complete and up-to-date documentation.

Responsibilities :

• Preparation, execution and documentation of IQ/OQ/PQ protocols.
• Participation in the validation life cycle: URS, DQ, FAT, SAT, FMEA, risk analyses.
• Engineering support for validation, requalification and maintenance programs.
• Drafting and revision of SOPs and technical documents.
• Management of activities related to quality systems: change control, deviations, CAPA.
• Contribution to the continuous improvement of the CQV program.

Profile :

• Bachelor’s degree in science or technical field.
• 5–10 years of experience in the pharmaceutical industry.
• Excellent skills in technical writing, organization and communication.
• Professional proficiency in German and English.

Gi Life Sciences contact :