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 if you have
* Knowledge of ISO 9001; ISO 13485; FDA, MDD/MDR, GMP
* 1-2 years experience
* Good communication skills - both oral and written
* Computer skills
* Product knowledge is desirable
What You'll Get
* Competitive Salary in accordance with experience and capabilities
* Pension
* Company performance bonus (paid annually)
* 33 days Holiday per year (incl Bank Holidays) plus Holiday Trading Scheme
* Benefits package: Life Assurance (x2), Income protection (50% of salary), Health Cashplan (Medicash), Benefit pot - for spending on additional benefits, which include: Upgrade Health Cash plan, Critical Illness cover, Cycle to work, Tech Benefits, Will Writing, Or add it to your pension pot if not used.
Applications close on Friday 7th March 2025