Process Engineer New

• Location: Cashel, Tipperary
• Type: Full-time | Permanent
• Salary: Competitive + Benefits

Join a leading pharmaceutical manufacturing site working on the development and commercialisation of inhalation products. This is a key role within the engineering team, focused on defining and delivering robust manufacturing processes for new and existing products.

• Lead engineering activities for new product introductions and process improvements.
• Collaborate with product development to ensure manufacturability is embedded in design.
• Create and manage User Requirement Specifications for manufacturing equipment.
• Plan and execute equipment validation activities.
• Manage project schedules and support capital expenditure planning.
• Provide hands-on technical support across Manufacturing and Packaging areas.
• Lead root cause investigations and implement CAPAs.
• Raise and manage Change Controls to closure.
• Review and approve batch documentation, procedures, protocols, and reports.
• Support continuous improvement initiatives and cross-functional collaboration.
• Drive new product and component introductions through structured engineering input.

• Degree in Engineering or Science (Mechanical/Manufacturing preferred).
• 5–8 years’ experience in a regulated manufacturing environment (Pharma/Medical Device ideal).
• Strong track record in equipment development, process validation, and troubleshooting.
• Solid understanding of GMP and regulatory standards (HPRA/FDA).
• Skilled in technical writing, presenting, and decision-making.
• Confident communicator who can work independently and in cross-functional teams.
• Experience with metered dose inhalation is an advantage.

Interested in making a real impact in a growing pharmaceutical facility?

Apply now or reach out directly for a confidential discussion.

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