Responsibilities: Support implementation and maintenance of QMS processes Administer eQMS system (QT9) Conduct audits and ensure compliance Train employees on QMS procedures Monitor performance and suggest improvements Provide backup for QA team admin tasks
Qualifications: BSc in a relevant scientific discipline or equivalent experience 5+ years of ISO13485 QMS experience 2+ years in IVD or medical device industry Knowledge of ISO13485, 21 CFR Part 820, and relevant regulations Strong communication and collaboration skills Experience with QMS systems and document control
The role requires a self-motivated individual with a strong attention to detail and ability to work across teams.
To be considered for this opportunity you will need to have the right to work in the UK.
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