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NIRAS Ireland is recruiting a Process Project Engineer to join our client’s engineering team in Westport, Mayo. You will manage a portfolio of processing equipment projects from cradle to grave, coordinating cross‑functional teams across operations, EHS and quality.
The role requires a third‑level engineering qualification and 2–5 years in pharma/biotech, with proven project management, supplier selection, and commissioning experience.
Project Engineer (Aseptic Pharma Manufacturing Environment)
Westport, Co. Mayo. Ireland
NIRAS Ireland provides Project Management, Engineering Design, and Project resourcing services to the Pharmaceutical and Life Science Sectors. As a company we specialize in the design and delivery of process‑driven projects across Ireland and internationally.
We are now recruiting a Process Project Engineer to join our client’s high performing Engineering team in Westport Co. Mayo. Successful candidate will join a team of 6, reporting to Sr. Manager and be responsible for a portfolio of small‑to‑large sized projects (20K to 15 million) related to new equipment/technologies and/or upgrades. Cross‑functional role – will support Operations, EHS and Quality departments and be responsible for 5‑6 projects at any one time – from cradle to grave. Projects may include installation of automated packaging lines or other equipment onsite; overseeing / securing funding, selection of vendors, installation (C&Q, validation, handover to relevant department).
The Project Engineer is responsible for safely coordinating and leading projects associated with Process Improvements, Automation, Aseptic processing, New Processing equipment with some Facility / Utilities Modifications to incorporate same. The primary responsibility of the role is to ensure that Projects meet their agreed goals/targets on time and on budget. The Project Engineer reports directly to the Senior Manager of Engineering who will give advice and support to ensure the equipment/facility/utilities design and goals/targets are achieved.
Be prepared to undertake any travel that the role may require for design review meetings, build inspections, Factory Acceptance Tests etc. This will be ad‑hoc (0‑4) times per year depending on business requirements.
Ideally seeking candidates holding qualifications in Mechanical/Electrical/Mechatronic Engineering with at least 3 years’ experience in a Pharma/Med Device Project Engineering or Process Engineering role with proven project management experience in a regulated manufacturing environment. Candidates will be working in a dynamic role – candidates must be self‑driven, able to multi‑task several projects and prioritise deliverables. Good understanding of assembly and processing equipment as well as facility/utility knowledge. Aseptic knowledge is not essential but a bonus.