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
1. Lead engineering activities for new product introductions and process improvements.
2. Collaborate with product development to ensure manufacturability is embedded in design.
3. Create and manage User Requirement Specifications for manufacturing equipment.
4. Plan and execute equipment validation activities.
5. Manage project schedules and support capital expenditure planning.
6. Provide hands-on technical support across Manufacturing and Packaging areas.
7. Lead root cause investigations and implement CAPAs.
8. Raise and manage Change Controls to closure.
9. Review and approve batch documentation, procedures, protocols, and reports.
10. Support continuous improvement initiatives and cross-functional collaboration.
11. Drive new product and component introductions through structured engineering input.
About You
1. Degree in Engineering or Science (Mechanical/Manufacturing preferred).
2. 5–8 years’ experience in a regulated manufacturing environment (Pharma/Medical Device ideal).
3. Strong track record in equipment development, process validation, and troubleshooting.
4. Solid understanding of GMP and regulatory standards (HPRA/FDA).
5. Skilled in technical writing, presenting, and decision-making.
6. Confident communicator who can work independently and in cross-functional teams.
7. 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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