CQV Engineer Job Description
We are recruiting for a CQV Engineer on behalf of a leading pharmaceutical company based in Cork. This is an initial 12-month contract role.
Key Responsibilities:
* Provide input into all aspects of C&Q, from design through to commissioning and qualification completion.
* Support and participate in the design of systems and equipment to ensure they comply with cGMP requirements.
* Prepare C&Q protocols as required (e.g., URSs/SRSs, Plans, Impact Assessments, DQ, IQ, OQ, PQ protocols and Reports).
* Review and approve documents prepared by contractor organisations (e.g., vendor SATs, FATs, commissioning protocols, project change controls/notifications).
* Track and support the resolution of Commissioning punch list items and Qualification deviations during the C&Q execution phase.
* Prioritize C&Q activities in line with site and project schedules.
Requirements:
* Third level degree and relevant experience.
* Minimum 5+ years experience in the Pharmaceutical (API) Industry.
* Experience of commissioning and qualifying some of the following systems: Reactors, Centrifuges, Dryers, Powder Handling Units, Skids, Vessels, Tanks, Pumps, Laminar Airflow Booths, autoclaves and isolators and clean / gray utility systems (such as purified water, water for injection clean steam, HVAC, Process Gases, Steam and Condensate systems etc.).
Estimated Salary Range: €70,000 - €90,000 per annum
About PE Global:
We are a leading recruitment agency specializing in the pharmaceutical industry. We are passionate about delivering exceptional recruitment solutions that meet our clients' needs.