PROCESS ENGINEER (VALIDATION ENGINEER)
Réalta Technologies is 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.
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.
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