Quality Engineer - Walsall
Opportunity:
Are you currently working as a quality engineer looking for your next role? Have you dealt with supplier quality assurance? Does your experience include incoming inspection of components/parts and customer returned goods? Looking for your next career move with an exciting global medical device company? If yes, then this is the role for you.
Your role as a Quality Engineer based in Walsall will involve working with the production team to ensure that the parts delivered from suppliers meet the design specifications and quality requirements. You will help production in supplier quality assessments including creating and following up on SCARs. You will ensure that the Device History Record (DHR) is up to date for the products manufactured. You will play a key role in ensuring the document control, CAPA, and complaints process is followed effectively.
Duties and responsibilities include:
1. Gatekeeper for all incoming parts/components.
2. Ensuring suppliers are meeting the quality standards as specified in supplier quality agreements.
3. Ensuring Production Feedback Reports, NCRs, and CAPAs are created for product and process issues found in Production.
4. Ensuring customer returns, document control, and complaint process is adhered to.
5. NCR/CAPA - Root cause analysis, monitoring of open NCR/CAPA's.
6. Change control - Monitoring of open change control, raising new change control.
7. Document control.
8. Risk Management of medical devices.
9. Supplier quality assurance development.
This is a full-time permanent job opportunity based in Walsall paying an excellent salary and great benefits such as 23 days holidays plus bank holidays on top, Insights Bonus scheme, cycle to work scheme, Life insurance, and much more.
Skills:
To apply for the role of Quality Engineer you will have the following:
1. Experience of working in a medical device industry as a quality engineer.
2. Working knowledge of ISO 13485 and ISO 14971.
3. Experience working with manufacturing/production in quality control.
4. Knowledge in processes for transition from EU MDD to EU MDR is a plus but not mandatory.
How to Apply:
To apply for this one-off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.
If this sounds like the role for you or a colleague then please don't hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.
For a list of our current vacancies, please visit the Quality Start website.
If you do not hear from Quality Start within 2 weeks your CV has not been shortlisted for this role.
Quality Start are acting as a specialist recruitment consultancy for this role.
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