Medical Device RA & QA Consultant — UK (Part-Time, ISO 13485)

ProPharma Group; Greater London; Hybrid; GBP 40,000 - 60,000; Part time

Job summary

A leading consulting firm is seeking a part-time RA / QA Consultant in West London. You will support ISO 13485 compliance and prepare documentation for clinical investigations. The ideal candidate has a robust background in medical device regulatory affairs and experience with ISO 13485 certification. This position offers a hybrid work model, valuing in-person collaboration through occasional on-site meetings.

Qualifications

• Strong background in medical device regulatory affairs is required.
• Experience with ISO 13485 certification is necessary.

Responsibilities

• Support ISO 13485 compliance.
• Prepare documentation for clinical investigations.
• Attend occasional on-site meetings.

Skills

Medical device regulatory affairs

ISO 13485 certification

Job description

A leading consulting firm is seeking a part-time RA / QA Consultant in West London. The role includes supporting ISO 13485 compliance and preparing documentation for clinical investigations. Ideal candidates will have a strong background in medical device regulatory affairs and experience with ISO 13485 certification. The position requires occasional on-site meetings, promoting a hybrid work model that values in-person collaboration.