Process Engineer- Biopharma client - Westmeath, Roscommon
Client:
PM Group
Location:
Roscommon, Ireland
Job Category:
Other
-
EU work permit required:
Yes
Job Reference:
b8abf73e1a50
Job Views:
4
Posted:
24.06.2025
Expiry Date:
08.08.2025
Job Description:
Overview PM Group is an international project delivery company operating across Europe, the USA and Asia. We provide project management, process design, facility design, construction management, and commissioning and qualification services for our leading multinational clients. In addition to managing large-scale one-off projects, at PM Group we also provide a Managed Service for capital projects to a growing number of clients. Our site-based Managed Service teams across Ireland provide a cost efficient and effective framework for project delivery to our clients. We take projects ranging in capital value from €100k to €15M from concept through all stages of the project life cycle to handover. PM Group is looking for a Process Engineer to join the Managed Services site-based team on a biopharma client site in Athlone, Co. Westmeath. We’re ideally looking for someone with fill-finish experience, given the nature of the facility and current project demands. Responsibilities • Work with Process engineers and Project Team on providing technical solutions for new/upgrade projects on existing systems and equipment. This will involve interaction with site Operations, EHS, Maintenance, Utilities, Technical and Quality teams, and SMEs, and ensuring that the proposed solutions are acceptable • Perform data analysis and make informed decisions/recommendations from conclusions reached based on the data • Liaise with Site Process Engineers, Maintenance, and Production to scope and define the business justification for upgrades to the plant/equipment • Project charters - develop high level descriptions of projects • Process descriptions - develop detailed descriptions of projects including: o Revisions to P&IDs, PFDs o Materials of construction o Sizing of equipment o Equipment and plant layouts o Control strategy and interlocks o Equipment datasheets • Writing User Requirement Specifications (URSs) • Participation in design reviews (Risk Assessments, HAZOPs, Safety & Environmental reviews, layout reviews, P&ID reviews, GA drawing reviews etc) • Working knowledge of automation • Documentation for Front End Loading (FEL) process for approval of capital expenditure • Close out detailed design queries with the project team (Piping Designer, Electrical, Instrumentation queries) • Supporting equipment procurement and attending FATs as required • Supporting the development of CAPEX plans. Qualifications • Bachelor of Engineering in Chemical or Process Engineering or equivalent discipline • 5 - 10 years' experience in biopharma / pharma sector • Fill-finish experience • Experience on GMP Process Equipment, CTU’s, Bioreactors, Centrifuges, Parts Washers • Awareness of process safety engineering and process safety management • Strong communication skills • Proactive and self-motivated • Capable of working independently or as part of a multi-disciplinary engineering team.
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