Senior Quality Assurance Specialist
A medical device organisation is seeking an experienced Senior Quality Engineer to play a key role in developing and maintaining their quality management system.
About the Role
* Develop, implement and continuously improve a compliant QMS aligned with ISO 13485 and FDA QS regulations.
* Support quality activities across design, development, manufacturing, risk management.
* Liaise with cross-functional teams for regulatory submission and approval.
Finding Success as Our New Team Member:
Bachelor's degree in Science or related field (minimum requirement).
The ideal candidate will have 5+ years' experience within Class II medical devices. Strong knowledge of IDO 13485 and FDA QRSExperience, including design control, risk management & audits.
The ability to operate efficiently in fast-paced environments will be highly regarded. Excellent communication skills are essential.
Please send your updated CV with relevant qualifications so we can progress further discussions regarding this opportunity.