Beschreibung
Specialist Associate Supplier Quality Engineer is needed to support remediation project with regards to new MDR regulations.
Requirements:
Management supplier's related Non-Conformities (NC's).
Ensuring timeline of NC closure and adequacy of corrective action as well as audit proof documentation
Management of supplier's related Corrective and Preventive Actions (CAPA's)
Management of supplier's change requests
Performance of product investigations
Supporting supplier's PFMEA
responsible for process verifications, validation, FMEA, Capability Studies
Prior experience in the medical device industries is required.
This is a contract role till end of Dec 2019.
Please call Beata Klecz on (see below) for further information
Michael Bailey International is acting as an Employment Business in relation to this vacancy.