CQV Engineer

CQV Engineer For our partner located in the canton of Valais, GI Life Science is looking for a: CQV Engineer Temporary position Your Mission: The CQV (Commissioning, Qualification, Validation) Engineer performs tasks related to the validation of equipment and facilities. This includes coordinating equipment installation, drafting IQ/OQ/PQ protocols, executing these protocols, and documenting the results in compliance with GMP requirements. Your Responsibilities: Participate in all validation activities (facilities and utilities, validation life cycle, execution and technical documentation, process, gap analysis, risk assessment). Validation deliverables include: URS (User Requirements Specification), DQ (Design Qualification), FMEA (Failure Mode and Effects Analysis), FAT/SAT (Factory and Site Acceptance Testing), and IQ, IOQ, OQ, PQ protocols. Prepare validation documentation. Execute IQ/OQ/PQ for equipment, systems, and utilities. Write reports on completed validation activities. Participate in Quality System activities: document management, change control, non-conformities, and CAPAs. Write or revise procedures related to engineering activities. Support the engineering team in preparing validation, requalification, and maintenance programs. Your Profile: Minimum Bachelor’s degree in a scientific or technical field. Fluent in German and English. Experience in the pharmaceutical industry. 5 to 10 years of experience in a similar position. jidd35ff10afr jit0624afr

Location: sitten-sitten, CH

Posted Date: 6/9/2025