Job Description
Join an established Quality Function, working with the QMS lead. This role will have broad responsibility for Documentation and QMS related maintenance.
Client Details
Our client is a Medical Device Manufacturer, working to MDR and ISO 13485 Standards.
Description
- Support the maintenance of QMS, through writing and assisting with SOPs, and other related documentation
- Support the broader QA/RA function as required
- Review batch records and help with release activities
Profile
- Basic understanding of QMS, within Medical Device or other regulated industry
- Educated in a related Scientific/Technical discipline
Job Offer
- Competitive salary, and benefits
- Strong supportive leadership
- Huge potential for career growth and development