QA/RA Specialist working at a class I & II medical device company specializing in needles and syringes. The ideal candidate can hit the ground running and work closely with their tight-knit Quality and Regulatory team. Daily responsibilities include:
- Writing technical files and SOPs
- Fulfilling post audit deliverables established by the auditors
- Has a deep understanding of the Quality Management System (QMS)
- CE Marking experience
Ideal candidate has worked in the Medical Device industry in Regulatory Affairs or Quality Assurance for a minimum of 2 years.
Sthree US is acting as an Employment Business in relation to this vacancy.