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Compliance manager

Stevenage
Bennett And Game Recruitment
Compliance manager
€55,000 a year
Posted: 27 April
Offer description

Overview

Position: Compliance Manager

Location: Stevenage

Salary: £50,000-£60,000 (dependent on experience)

Compliance Manager required for our client based in Stevenage, a rapidly growing UK-based health tech start-up building wearable technology to support people living with neurological conditions.

They are looking for a Compliance Manager to own our compliance roadmap end-to-end: building and maintaining a compliant QMS (ISO 13485-aligned), managing certification / technical documentation for UKCA / CE (UK / EU), coordinating FCC for the US market, and leading external audits and test houses.

This role sits at the interface of engineering, operations, suppliers, and regulatory consultants / notified bodies (where needed). You will ensure our documentation, processes, and evidence are audit-ready and proportionate to the company's stage.


Responsibilities

* Own our regulatory plan for UKCA (UK), CE marking (EU), and FCC (US), aligned to product claims, intended use, risk classification, and target markets.
* Maintain a compliance matrix covering applicable standards and regulations (e.g., EMC, electrical safety, biocompatibility if relevant, labelling / IFU, UDI where applicable).
* Coordinate with external test labs, regulatory consultants, and (if applicable) Notified Bodies / UK Approved Bodies.
* Ensure product marketing claims remain consistent with regulatory positioning and evidence.
* Design, implement, and maintain a Quality Management System suitable for a medical device manufacturer (typically ISO 13485; with ISO 9001 where useful).
* Own and maintain the product Technical File / Technical Documentation, ensuring it is complete, current, and defensible.
* Ensure traceability from requirements → risk controls → verification / validation → release.


Qualifications

* Experience leading ISO 13485 (or equivalent medical-device QMS) implementation and / or maintenance, including external audits.
* Strong working knowledge of UKCA / CE regulatory pathways for medical devices and associated technical documentation expectations.
* Experience coordinating EMC / radio / safety testing and managing third-party test houses.
* Practical experience with CAPA, document control, change control, supplier quality, and complaint handling.


Salary & Benefits

* Salary - £50,000-£60,000 (dependent on experience)
* Monday to Friday (09:00 to 17:00)
* On-site position
* Holiday package
* Pension scheme
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