At a Glance
- Tasks: Lead quality management for ISO 13485 and ensure top-notch standards in medical devices.
- Company: Specialist medical device manufacturer focused on innovative neonatal solutions.
- Benefits: Flexible remote work, clear career progression, and involvement in regulatory affairs.
- Other info: Join a dynamic team with opportunities for professional growth and impact.
- Why this job: Make a real difference in healthcare while advancing your career in a growing field.
- Qualifications: Experience in quality management and knowledge of ISO 13485 standards.
The predicted salary is between 51750 - 63250 £ per year.
Cure Talent are partnering with a specialist medical device manufacturer whose portable neonatal incubators are deployed in challenging environments across global markets. As Quality Manager, you will own the ISO 13485 QMS and lead quality across the business, based in Stevenage, Hertfordshire with two days per week working from home.
This role offers a defined growth path into regulatory affairs and potential PRRC responsibility as the business scales, with early involvement in MDR/Notified.
MedTech Quality Manager: ISO 13485 Lead, Remote 2 days/wk in Stevenage employer: Cure Talent
Join a leading global medical device company that is dedicated to innovation and excellence in life-saving technologies. As a Senior Regulatory Affairs Specialist, you will thrive in a collaborative work culture that values mentorship and continuous improvement, while enjoying opportunities for professional growth in a dynamic environment. Located in a vibrant area, this role offers the chance to make a meaningful impact on product portfolios and regulatory strategies, ensuring your contributions are recognised and valued.
