Process Engineer – Inhalation Manufacturing
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.
Key Responsibilities
* 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.
About You
* 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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