LSC are currently looking for a C&Q Engineer to join a Capital Projects team with our multinational Biopharma client in Cork.
The C&Q Engineer will commission and/or qualify site equipment systems such as skids, vessels, bio-reactors, temperature controlled units and utility systems (such as water, clean steam, HVAC, process gases)
The C&Q Engineers main responsibilities would are:
oProvide input into all aspects of validation i.e. from design through to the commissioning and qualification execution phases
oParticipate in the design of systems and equipment to ensure that they comply with GMP requirements. Develop validation documentation as required (e.g. specifications, plans, protocols, procedures).
oReview and approve documents prepared by the validation team, other departments and contractor organisations (e.g. commissioning test plans, impact assessments, change controls).
oExecute qualification protocols as required.
oCompile relevant documentation from contractors, suppliers, and other departments for inclusion in reports.
oPrepare reports of executed protocols for review by QA.
The C&Q Engineer wil have:
oMinimum 3+ years’ experience in the Pharmaceutical Industry.
oExperience on commissioning, qualifying / verifying some of the following systems: Utilities (water for injection, clean steam, process gases, HVAC), fridges, freezers, LAF, BSC units, autoclaves and isolators.
Call James in LSC 021 4777 329 for more details on this new C&Q Engineer role or apply directly via this advert.