Im currently supporting an innovative MedTech company based in Grenoble in the search for a Supplier Quality Manager.
This role is within a pioneering company developing an active implantable medical device addressing major unmet needs in urology. The technology has the potential to significantly improve patients quality of life.
Key responsibilities include
Defining and implementing supplier quality processes
Supplier qualification and quality agreements
Supplier audits and process validation oversight
Managing supplier non-conformities and quality documentation
Working closely with industrial R&D and quality teams
Profile sought
MSc / Engineering degree in Quality Engineering or similar
7 years experience in Quality / Supplier Quality in Medical Devices
Strong knowledge of ISO 13485 and 21 CFR 820
Experience with supplier audits and process validation
Fluent English
Location: Grenoble France.
If you are interested or know someone who could be a great fit feel free to reach out or send me a message.
Im currently supporting an innovative MedTech company based in Grenoble in the search for a Supplier Quality Manager. This role is within a pioneering company developing an active implantable medical device addressing major unmet needs in urology. The technology has the potential to significantly im...
Im currently supporting an innovative MedTech company based in Grenoble in the search for a Supplier Quality Manager.
This role is within a pioneering company developing an active implantable medical device addressing major unmet needs in urology. The technology has the potential to significantly improve patients quality of life.
Key responsibilities include
Defining and implementing supplier quality processes
Supplier qualification and quality agreements
Supplier audits and process validation oversight
Managing supplier non-conformities and quality documentation
Working closely with industrial R&D and quality teams
Profile sought
MSc / Engineering degree in Quality Engineering or similar
7 years experience in Quality / Supplier Quality in Medical Devices
Strong knowledge of ISO 13485 and 21 CFR 820
Experience with supplier audits and process validation
Fluent English
Location: Grenoble France.
If you are interested or know someone who could be a great fit feel free to reach out or send me a message.
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