FULL TIME
Cork, Ireland
Process Engineer (Validation Engineer)
Réalta Technologies are looking for a Process Engineer (Validation Engineer), this role sits within a specialist engineering team supporting the development and manufacture of innovative medical device solutions.
The Process Engineer will provide technical and validation support across manufacturing and project activities, driving process improvements, ensuring compliance, and supporting the introduction of new products and technologies.
Key Responsibilities
Lead and support process validation activities (IQ, OQ, PQ) and maintain compliant documentation
Provide engineering input for new product and process introductions
Drive continuous improvement initiatives to enhance quality, cost, and efficiency
Support troubleshooting, root cause analysis, and implementation of corrective actions
Develop and maintain SOPs, work instructions, and other GMP documentation
Collaborate with cross-functional teams and external partners to deliver on project goals
Ensure all work complies with Quality and EHS requirements.
Qualifications & Skills
Level 7/8 Degree in Mechanical, Process, or related Engineering discipline.
2–4 years' experience in a regulated manufacturing or medical device environment.
Strong understanding of process validation and Six Sigma or problem-solving tools.
Proven project management and analytical skills.
Excellent communication and collaboration skills.
Self-motivated, adaptable, and technically curious.