Project Engineer - Process (Biotech) - PM Group
  • Limerick, County Limerick, Ireland
  • via ClickaJobs (1)
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Job Description

Overview Who we are: PM Group is an employee-owned, international project delivery firm with a team of 3,700+ people. We are world leaders in the pharma, food, medtech, and mission critical sectors. From our network of offices in Europe, Asia, and the US, we work with the world's leading organisations. We are focused on growing a sustainable business centred around our people, our clients, and trade partners. PM Group has an opportunity for an experienced Project Engineer - Process (Biotech) for our leading client based in Limerick. The successful candidate will have suitable experience in the Biopharma Industry. Responsibilities Main responsibilities will include: Reviews and approves system lifecycle documentation (FS, SDS, IO lists, etc.) and ensures they meet requirements. Generation of User Requirement Specification (URS) for assigned systems. Reviews and approves Basis of Design (BOD) and detail design of assigned systems i.e. PFDs, P&IDs, etc. Ensures procurement packages (bill of materials (BOM), datasheets, cutsheets, etc.) meet equipment specifications. Attends factory acceptance test (FAT) of associated equipment if required. Attends automation software bench FAT if required. Supervises and executes Site Acceptance Testing (SAT) and commissioning activities. Ensures Vendor Document Requirements (VDR) meet requirements. Builds Preventative Maintenance (PM) tasks and spare parts lists on Computerised Maintenance Management System (CMMS). Generates FAT, SAT, and commissioning protocols for assigned equipment and ensures protocols meet specifications. Qualifications Experience & Skills Engineering 3rd level qualification (Chemical, Process Engineering, or equivalent). Show proven expertise in the provision of personnel to meet the requirements. Supply proven SME’s for the assigned tasks and areas. Have sufficient staff available with the relevant skills for the project. Project and/or operations experience within a process or biopharmaceutical cGMP regulated environment. Experience of bioprocessing equipment specification, commissioning, and operation. #J-18808-Ljbffr

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