Regulatory Affairs Specialist

CV-Library
Derby, Derbyshire
12 months ago
Applications closed

Related Jobs

View all jobs

Regulatory Affairs Specialist

Cure Talent Didcot, United Kingdom

RA Specialist

GxPeople Global United Kingdom
£40,000 – £50,000 pa Remote

Regulatory Affairs Apprentice

Smith & Nephew United Kingdom

QA/RA Officer

Genedrive Manchester, United Kingdom

Internal Auditor - Public Sector Services

Newton Colmore Cannock, WS11 1DD, United Kingdom

Physicist - Fluidics Research

Newton Colmore Cambridge, United Kingdom
Posted
7 May 2025 (12 months ago)

Cranleigh STEM is working with a market-leading chemical manufacturer who are at the forefront of materials innovation across Europe. Based in Derby, our client delivers high-performance solutions to a wide range of industries. They are now seeking an experienced Regulatory Affairs Specialist to ensure continued regulatory compliance across their European business, with a particular focus on chemical safety, transportation, and emerging legislation.

This is a critical role supporting both operational compliance and long-term business continuity. You’ll work cross-functionally across regulatory, R&D, supply chain and logistics to ensure that product documentation and processes meet current UK and EU requirements, particularly in line with REACH, CLP, and other relevant frameworks.

Regulatory Affairs Specialist responsibilities:

Author, review and maintain Safety Data Sheets (SDS) for European products in compliance with UK and international chemical regulations

Ensure adherence to UK REACH, EU REACH, GB and EU CLP, and PIC regulations, as applicable to the European business

Prepare and submit Poison Centre Notification (PCN) dossiers; ensure compliance with relevant member state requirements

Monitor chemical regulatory landscapes for potential risks and restrictions that may impact the business

Advise logistics teams on the transport of dangerous goods under applicable legislation (ADR, IATA, IMDG, etc.)

Liaise with external regulatory consultants to manage ongoing compliance projects and submissions

Partner with R&D teams to review new materials and formulations from a regulatory perspective

Coordinate with supply chain teams to obtain regulatory information from vendors and maintain up-to-date records

Apply the Carlisle Operating System (COS) methodologies across compliance tasks and improvement initiatives
Regulatory Affairs Specialist requirements:

Bachelor's degree in Chemistry, Polymer Science, Toxicology or closely related field of study.

Strong working knowledge of GHS, REACH (UK & EU), and SDS authoring practices

Demonstrated experience with GB HSE and EU ECHA compliance processes and documentation

Excellent communication skills, with the ability to work effectively across multidisciplinary teams in both the UK and Europe

Experience with Sphera Intelligent Authoring software is desirable
You’ll be joining a highly respected business with a strong European footprint, committed to safety, innovation and compliance excellence. With a collaborative working environment and a robust operational framework, the company offers opportunities for both professional growth and meaningful impact.

£Comp + relocation assistance + excellent company benefits

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Where to Advertise Medical Technology Jobs in the UK (2026 Guide)

Advertising medical technology jobs in the UK requires a different approach to most technical hiring. The medtech candidate pool spans biomedical engineers, regulatory affairs specialists, clinical scientists, software engineers working within IEC 62304 and MDR frameworks, imaging scientists and commercial professionals with deep healthcare sector knowledge. General job boards consistently conflate medical technology with broader healthcare, pharmaceutical and IT roles — producing high application volumes but low candidate quality for specialist medtech positions. This guide, published by MedicalTechnologyJobs.co.uk, covers where to advertise medical technology roles in the UK in 2026, how the main platforms compare, what employers should expect to pay, and what the data says about hiring across different role types.

How Many Medical Technology Tools Do You Need to Know to Get a Medical Technology Job?

If you’re pursuing a career in medical technology, it can feel like the toolkit is endlessly long: imaging systems, data analysis software, regulatory platforms, testing frameworks, prototyping tools, CAD, quality management systems, signal processing libraries and more. Scroll job boards or LinkedIn, and it’s easy to think you need to know every tool under the sun just to secure an interview. Here’s the honest truth most hiring managers won’t explicitly tell you: 👉 They don’t hire you because you know every tool — they hire you because you understand the underlying principles and can apply the right tool in the right context to solve real problems. Tools matter — absolutely — but they are secondary to problem-solving ability, clinical awareness, engineering rigour and the ability to deliver safe, reliable solutions. So how many medical technology tools do you actually need to know to get a job? For most job seekers, the answer is far fewer than you think. This article explains what employers really want, which tools are core, which are role-specific, and how to focus your learning so you look confident, competent and end-game ready.

What Hiring Managers Look for First in Medical Technology Job Applications (UK Guide)

Medical technology (MedTech) is one of the most dynamic and high-impact sectors in the UK — spanning medical devices, diagnostics, digital health, AI-assisted systems, wearables, imaging, robotics and clinical software. At the same time, hiring managers are exceptionally selective because MedTech roles demand technical excellence, regulated safety awareness, clinical context and cross-disciplinary collaboration. Whether you’re applying for roles in R&D, engineering, quality & regulatory, clinical validation, product management or software development for medical systems, hiring managers don’t read every word of your CV. They scan it quickly — often deciding within the first 10–20 seconds whether to continue reading. This guide breaks down exactly what hiring managers look for first in medical technology applications — and how you can make your CV, portfolio and cover letter stand out in the UK market.