Quality & Regulatory Affairs Lead: ISO 13485 & MDSAP in Bristol

Quality & Regulatory Affairs Lead: ISO 13485 & MDSAP in Bristol

Bristol Part-Time 30000 - 40000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead regulatory activities and maintain quality management systems in a dynamic environment.
  • Company: Join Natracare, a people-centred, employee-owned business in Bristol.
  • Benefits: Enjoy robust employee benefits and a flexible part-time hybrid setup.
  • Other info: Be part of a mature QMS environment that values continuous improvement.
  • Why this job: Make a real impact on quality assurance and regulatory affairs in a supportive team.
  • Qualifications: Experience in Quality Assurance and Regulatory Affairs, especially ISO 13485 & MDSAP.

The predicted salary is between 30000 - 40000 £ per year.

Natracare (Bodywise UK Ltd) is seeking an experienced Quality Assurance and Regulatory Affairs professional to lead regulatory activities, maintain QMS, and drive continuous improvement within a people‑centred, employee‑owned business. The role is part‑time in a hybrid setup based in Bristol and offers robust employee benefits.

You will manage regulatory submissions, maintain the DMR and SOPs, and support Notified Body audits while working in a mature QMS environment that prioritises health.

Quality & Regulatory Affairs Lead: ISO 13485 & MDSAP in Bristol employer: Natracare

Natracare is an exceptional employer that values its employees through a people-centred approach and offers a supportive work culture in a hybrid setup based in Bristol. With robust employee benefits and opportunities for professional growth, you will thrive in a mature Quality Management System environment that prioritises health and continuous improvement, making your contributions impactful and rewarding.

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Contact Details:

Natracare Recruitment Team

We think you need these skills to ace Quality & Regulatory Affairs Lead: ISO 13485 & MDSAP in Bristol

Quality Assurance
Regulatory Affairs
ISO 13485
MDSAP
Quality Management System (QMS)
Regulatory Submissions
Document Management Record (DMR)