Quality & Regulatory Manager in Perivale

Energy Jobline ZR; City Of London; On-site; GBP 60,000 - 80,000; Full time

Job summary

A global energy job board seeks a Quality and Regulatory Manager to lead quality strategy and ensure compliance in the medical device sector. The role involves managing audits and driving continuous improvement across international markets. Ideal candidates will have a degree in Life Sciences or Engineering and relevant experience in regulatory compliance. A background in dermatology or microbiology is a bonus.

Qualifications

• Proven experience in leading quality and regulatory strategy in the medical device sector.
• Strong understanding of ISO 13485-compliant Quality Management Systems.
• Ability to ensure global regulatory compliance across multiple markets.

Responsibilities

• Oversee ISO 13485-compliant Quality Management System.
• Manage audits, CAPAs, and post-market surveillance.
• Act as designated PRRC under EUMDR 2017/745.

Skills

Experience in medical device regulatory compliance

Degree in Life Sciences or Engineering

Experience with international submissions (UK/EU/US/Canada)

Background in Dermatology or microbiology

Education

BSc/BEng in Life Sciences or Engineering

Job description

Overview

Energy Jobline is the largest and fastest growing global Energy Job Board and Energy Hub. We have an audience reach of over 7 million energy professionals, 400,000+ monthly advertised global energy and engineering jobs, and work with the leading energy companies worldwide.

We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.

Job Description

Are you an experienced QA/RA professional ready to lead quality and regulatory strategy in the medical device space?

We're looking for a Quality and Regulatory Manager to oversee our ISO 13485-compliant Quality Management System and ensure global regulatory compliance across UK, EU, US, and Canadian markets. You'll be the designated PRRC under EUMDR 2017/745 and play a key role in driving continuous improvement, managing audits, CAPAs, and post-market surveillance.

What You'll Bring

• Degree in Life Sciences or Engineering (BSc/BEng)
• Experience in medical device regulatory compliance
• Experience with international submissions (UK/EU/US/Canada)
• Bonus: Dermatology or microbiology background

Why Apply?

• Lead a high-impact team (2 direct reports)
• Shape quality culture across the business
• Collaborate with global partners and suppliers
• Drive innovation in a growing medical device company

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy

If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.