Senior Medical Device Regulatory & Quality Consultant

ARx Recruitment Services; United Kingdom; Hybrid; GBP 100,000 - 125,000; Full time

Job summary

A reputable consultancy in the medical device sector is seeking experienced Consultants and Senior Consultants to guide clients through regulatory submissions and quality management systems. Candidates should have proven expertise in Quality Assurance and Regulatory Affairs, working independently and collaboratively. This position offers a flexible, project-based role with competitive remuneration.

Benefits

Flexible project-based role

Competitive remuneration

Qualifications

• Proven experience in Quality Assurance and/or Regulatory Affairs within Medical Devices or IVDs.
• Strong understanding of international regulatory requirements (CE, FDA, MHRA, NICE, etc.).
• Ability to work independently with minimal oversight.

Responsibilities

• Advise clients on CE marking and FDA submissions.
• Provide practical support to ensure compliance.
• Implement and maintain Quality Management Systems.

Skills

Quality Assurance

Regulatory Affairs

Client Management

Problem-Solving

Job description

A reputable consultancy in the medical device sector is seeking experienced Consultants and Senior Consultants to guide clients through regulatory submissions and quality management systems. Candidates should have proven expertise in Quality Assurance and Regulatory Affairs, working independently and collaboratively. This position offers a flexible, project-based role with competitive remuneration.