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Hire regulatory affairs specialist (medtech)s in the UK

What regulatory affairs specialist (medtech)s are paid, what to name in the advert, and who you are up against — from the adverts on Medical Technology Jobs, not a survey. Looking for the roles themselves? See Regulatory Affairs Specialist (MedTech) jobs.

What you will pay

£35k to £60k, most around £47k

The range employers advertised for regulatory affairs specialist (medtech)s on Medical Technology Jobs over the last 12 months, base salary only, across 14 priced adverts. Adverts that state a salary get more applications than those that hide it, and a figure at or above the midpoint is the single cheapest thing you can do for the response.

Remote or anchored

A fully remote role draws the whole country and can pay a little under the London figure; an anchored one competes locally and cannot.
Greenfield or inherited

Building from nothing is worth more to the right person than running what exists, and they will ask which it is.
Someone senior to learn from

A strong lead in the team is worth thousands on the offer; without one, expect to pay for that experience directly.

Who you are competing with

Hiring regulatory affairs specialist (medtech)s on Medical Technology Jobs right now

Newton Colmore 1

Three live adverts for the role, as candidates see them. How rivals pitch it is worth a look before you write yours.

Newton Colmore · 11–50 people

Regulatory Affairs Specialist - Medical Devices - Cambridge

Cambridge
Mid-level

Provide regulatory support across a Cambridge product development business, guiding multidisciplinary engineering and science teams on compliance with ISO 9001, ISO 13485 and FDA 21 CFR 820. Monitor international regulatory changes, support external audits and contribute to quality management system improvements across medical and non-medical projects.

3 weeks ago

L-ev8 Recruitment Ltd

Senior Quality & Regulatory Affairs Specialist

Burgess Hill
£50,000 pa
Senior
Part time

Part-time role maintaining quality and regulatory compliance for a Class I(s) medical device manufactured by an approved contract manufacturer. You will oversee supplier quality, review batch documentation, validation and change control, maintain technical files, and support audits, vigilance and post-market surveillance, working closely with the Head of Quality and sharing PRRC responsibilities.