Validation Engineer | Longford | Medical Device Jobs Ireland | Onsite
About the Company
Our client is a leading medical device manufacturer based in Longford, working with global healthcare organisations to deliver high-quality, innovative products.
The company is currently going through an exciting growth phase and is expanding its technical team, offering excellent opportunities for career development within a highly regulated manufacturing environment.
About the Role
This onsite Validation Engineer job in Longford supports new product introductions and validation activities within a regulated medical device manufacturing environment.
Reporting to the Validation Manager, you will execute validation protocols, support change control, and ensure compliance with ISO 13485 and GMP standards, while driving continuous improvement.
This Validation Engineer role offers an excellent salary, strong benefits, and clear career progression opportunities.
Responsibilities
- Develop and execute validation protocols and reports for new product introductions and revalidations
- Maintain compliance with ISO 13485 and GMP standards
- Support change control processes across validated systems
- Perform risk assessments and root cause analysis (FMEA, 5 Whys)
- Support regulatory and internal audits
- Analyse data using statistical tools (Minitab, SPC)
- Collaborate with cross-functional teams and external vendors
Requirements
- Degree in Engineering, Polymer Science, or related discipline
- 2+ years’ experience in a Validation Engineer role within a regulated manufacturing environment
- Experience in medical devices, pharma, or similar industries
- Strong knowledge of validation, GMP, and quality systems
- Experience with Minitab, SPC, and risk management tools
- Excellent written and verbal English communication skills
What’s Next
If you’re interested in this Validation Engineer job in Longford or other medical device jobs in Ireland, apply now or contact Tina at Sigmar for a confidential discussion
