Overview
Process Engineer – Medical Devices
Sheffield (site-based)
We are supporting a well-established and growing manufacturer within the medical devices sector who are looking to appoint a Process Engineer at their Sheffield site.
This is an excellent opportunity to join a highly regulated environment where you’ll play a key role in supporting manufacturing operations, driving continuous improvement, and leading validation activities across the business.
Key responsibilities:
1. Deliver process validation activities (IQ, OQ, PQ) for new and existing processes
2. Support manufacturing and process development activities on site
3. Identify and implement continuous improvement initiatives (Lean / Six Sigma)
4. Work cross-functionally to improve production efficiency and product quality
5. Ensure compliance with ISO 13485 and quality management systems
What we’re looking for:
6. Experience in a Process or Manufacturing Engineering role within medical devices or a similar regulated industry
7. Strong background in validation and continuous improvement projects
8. Good understanding of manufacturing processes
9. Knowledge of ISO 13485 or equivalent quality standards
10. Strong analytical and problem-solving skills
This is a site-based role offering the chance to contribute to impactful projects within a collaborative and forward-thinking environment.
For more information or a confidential discussion, please apply or get in touch directly.
Apply
Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy
Find our privacy policy here