Job Description
Become Part of the Team
With over 35 years of experience, Flexicare is a leading designer and global provider of medical devices that enhance patient care. Headquartered in the UK, we support clinicians worldwide with class-leading devices and a global network of subsidiaries across over 100 countries. Flexicare has ambitious plans for international growth and we want you to be a part of our journey!
What You'll Do
Ensure products and processes compliance is maintained on the following: ISO 13485, ISO9001; FDA; MED DEV
93/42/EEC and MDR 2017/745 (when applicable) and any other regulatory compliance required by the business
along with customer requirements.
* Complaint Intake
* Complaint investigation follow up
* Decontamination process maintenance
* Q-Pulse record maintenance
* Authority to stop batch/line production pending investigation of quality issues/non-conforming product.
* Use of test equipment, both electronic and mechanical.
* Adhere to company procedures in line with good documentation, manufacturing and engineering practices.
* Improvement/reduction in complaint KPIs
* Improvement/reduction in complaint investigation processes
Who You Are
We believe you're the right fit ...