Description
Quality Engineer - Manchester or Remote - Medical Devices - Contract (9 Months) - Immediate Start
G2's medical devices client based in Manchester are currently looking for a Quality Engineer to join their team for the next 9 months.
Essential Skills:
- ISO:13485 experience
- Root cause investigation and action completion (CAPA)
Desirable Skills:
- FDA 21 CFR 820 experience
Main Job function includes:
- Complaint investigation
- Non-conformance Management
- Supplier Management (including SCAR management)
- Incoming and outgoing Product Inspections, product documentation reviews, Product release.
- Root Cause Analysis
- Maintaining & managing QMS documentation & procedures (review/revision/writing new procedures & work instructions) using the eQMS system
- Liaising with other departments (Customer Service, Sales & marketing, Clinical)
Title: Quality Engineer
Location: Manchester (or remote)
Rate: Negotiable (dependant on experience; to be discussed on the phone)
Type: Contract (9 Months)
If you have the skills and experience required, please send an updated version of your CV
g2 Recruitment are committed to equality of opportunity for all applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships or any other characteristic protected by law.