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Overview
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 now has an opportunity for a Process Engineer to work with a biopharma client based in Limerick.
Responsibilities
1. Reviews and approves system lifecycle documentation (FS, SDS, IO lists, etc.) and ensures they meet requirements.
2. Generates User Requirement Specification (URS) for assigned systems.
3. Reviews and approves Basis of Design (BOD) and detail design of assigned systems i.e. PFDs, P&IDs, etc.
4. Ensures procurement packages (bill of materials (BOM), datasheets, cutsheets, etc.) meet equipment specifications.
5. Attends factory acceptance test (FAT) of associated equipment if required.
6. Attends automation software bench FAT if required.
7. Supervises and executes Site Acceptance Testing (SAT) and commissioning activities.
8. Ensures Vendor Document Requirements (VDR) meet requirements.
9. Builds Preventative Maintenance (PM) tasks and spare parts lists on Computerised Maintenance Management System (CMMS).
10. Generates FAT, SAT and commissioning protocols for assigned equipment and ensures protocols meet specifications.
Qualifications
1. Engineering 3rd level qualification (Chemical, Process Engineering or equivalent).
2. Show proven expertise in the provision of personnel to meet the requirements.
3. Supply proven SME’s for the assigned tasks and areas.
4. Have sufficient staff available with the relevant skills for the project.
5. Project and/or operations experience within a process or biopharmaceutical cGMP regulated environment.
6. Experience of bioprocessing equipment specification, commissioning, and operation.
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