Senior Regulatory & Quality Consultant – Medical Devices

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

Job summary

A healthcare consultancy in the UK is seeking Consultants and Senior Consultants in Quality Assurance and Regulatory Affairs. The role involves guiding clients in the medical device and IVD sectors through regulatory submissions and compliance strategies. Ideal candidates will have proven experience and a strong understanding of international regulations. The position offers competitive remuneration and a flexible, project-based working environment.

Benefits

Flexible working hours

Collaborative team environment

Competitive remuneration based on experience

Qualifications

• Proven experience in Quality Assurance and Regulatory Affairs within Medical Devices or IVDs.
• Strong understanding of international regulatory requirements.
• Ability to work independently with minimal oversight.

Responsibilities

• Advise clients on CE marking, FDA submissions, and other regulatory pathways.
• Provide practical support to ensure compliance with international requirements.
• Implement and maintain Quality Management Systems.

Skills

Quality Assurance

Regulatory Affairs

Problem-solving

Client management

Job description

A healthcare consultancy in the UK is seeking Consultants and Senior Consultants in Quality Assurance and Regulatory Affairs. The role involves guiding clients in the medical device and IVD sectors through regulatory submissions and compliance strategies. Ideal candidates will have proven experience and a strong understanding of international regulations. The position offers competitive remuneration and a flexible, project-based working environment.