Compliance Administrator

Basingstoke
1 week ago
Create job alert

Job - Compliance Administrator (Compliance Support)

The client customer are a leading technological innovator and supplier of Aircare (fragrance delivery systems and consumables) & functional hygiene products in a number of industry sectors, a worldwide and renowned for delivering sanitary and scent solutions to over 130 countries.

Provide Compliance support to the Product Development/Sales teams both UK and US and working closely with Compliance Lead Position Overview:

To support the Compliance Manager in managing the regulatory aspects of all Vectair products ensuring the business meets the legislation and regulatory requirements in UK, EU, US and Rest of World (ROW).

Supporting the business sustainability aims by submitting and tracking documentation for applications such as carbon footprint and plastic tax.

The Compliance Administrator will:

Provide guidance on labelling compliance (GB/EU CLP, OSHA, GHS), including label proofreading.

Help ensure technical and marketing claims are accurate and compliant.

Maintain key documentation such as ISO, CoA, CoC, CE, and UKCA records from manufacturing partners.

Create and maintain SDS using Formpak software in line with applicable REACH, OSHA, and Canadian GHS requirements.

Track and manage SDS updates through Wrike project management software.

Use Helix and ECHA tools to help monitor and research emerging regulations, as well as communicating with manufacturing suppliers.

To assist the R&D Department as and when necessary.

Day to day activities will include (Global business):

SDS creation:

Create SDS for Vectair- branded and OEM/Private label (Customer Bespoke) products.

Set up raw materials and mixtures in Formpak.

Generate and assign UFI numbers

Prepare i6Z files for EU poison centre notifications.

Maintain the master poison centre list

Product labels:

Proofread product labels to ensure labels are compliant with labelling regulations such as CLP, OSHA, GHS, by proofreading labels to certify that they match their SDS.

Compliance / Regulations:

Assist in monitoring changes to legislation (REACH, RoHS, CE, FCC, UKCA, CLP, Prop 65, California Right to Know etc.

Communicating any findings with the Compliance Manager.

Upload data in Helix.

Liaise with suppliers for ISO certification, maintain certification database ensuring when documents have expired, we have a new copy.

Documentation and Customer Support:
Provide documents such as CoAs, CoCs, and draft declarations for Compliance Manager review.

Respond to internal queries and assist the Customer Support department with compliance-related documentation.

Experience/qualifications required:

Strong organisational skills.

Attention to detail and the ability to proof check.

Experience with Microsoft Office,

Intermediate Excel skills

Picks up database systems with ease.

Experience in regulatory affairs would be advantageous.

Experience using SDS software such as Formpak or similar would be advantageous.

Some experience with GHS, CLP, OSHA and Reach would be advantageous

Some experience with ECHA website would be advantageous

Can work as part of a team or on their own.

Experienced in the use of Adobe Acrobat Pro.

Software Tools Used in This Role:

Formpak – SDS creation and management

Wrike – Task and workflow tracking

Helix – Chemical and regulatory database

ECHA – Research and regulatory updates

Office 365 – Communication and documentation

Related Jobs

View all jobs

Product Documentation Administrator

Applications Support Manager

BOM Analyst x 4

Customer Service Engineer

Customer Service Engineer

Customer Service Engineer

Get the latest insights and jobs direct. Sign up for our newsletter.

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

Industry Insights

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

Contract vs Permanent Medical Technology Jobs: Which Pays Better in 2025?

Medical technology—often called “MedTech”—continues to revolutionise how healthcare is delivered, monitored, and managed. From AI-powered imaging and wearable health sensors to robotic surgery systems and sophisticated patient data platforms, MedTech is fueling an era of personalised, efficient, and preventive medicine. In the United Kingdom, this sector is expanding rapidly, driven by a blend of cutting-edge research, public and private investment, and increasing demand for healthcare innovations. With such growth comes a variety of high-paying job opportunities. MedTech professionals—from regulatory specialists and software developers to biomedical engineers and clinical project managers—face a critical decision: Should they contract on a day rate, commit to a fixed-term contract, or secure a permanent position? Each path offers distinct advantages, trade-offs, and implications for earning power. This comprehensive guide examines these three primary employment models within the UK’s medical technology sector, highlighting potential salary ranges, pros and cons, and realistic examples of how your take-home pay could differ. Whether you are seeking short-term gains, long-term growth, or a balance of both, this article will help you weigh your options and plan your next career move in 2025.

Medical‑Technology Jobs for Non‑Technical Professionals: Where Do You Fit In?

Innovating Healthcare Beyond the Circuit Board From AI‑enabled imaging at Moorfields to remote‑monitoring wearables on NHS wards, medical technology (med‑tech) is Britain’s fastest‑growing life‑sciences sub‑sector. The Association of British HealthTech Industries (ABHI) reports that UK med‑tech sales hit £30 billion in 2024, supporting 154,000 jobs—yet headlines still glorify software developers and biomedical engineers. The reality? Almost 40 % of open med‑tech vacancies prioritise regulatory, commercial and operational expertise over pure engineering (ABHI UK HealthTech Talent Survey 2024). If you excel at compliance, project delivery, storytelling or health‑economic modelling, this guide shows where you fit in—no scalpel or Python required.

CMR Surgical Jobs in 2025: Your Complete UK Guide to Building the Versius Surgical Robot & Transforming Minimal‑Access Surgery

K‑based CMR Surgical has gone from Cambridge start‑up to global surgical‑robotics heavyweight in little more than a decade. Its flagship Versius Surgical System is now in daily use across Europe, Asia‑Pacific, Latin America—and, as of October 2024, the United States following FDA marketing authorisation. (us.cmrsurgical.com) Around the same time CMR secured a new £160 m (~$200 m) funding round, bringing total investment to $1.32 bn and creating a fresh wave of hiring for 2025. (tracxn.com) Whether you are a graduate engineer, a clinical trainer with operating‑theatre experience, or a field‑service guru who keeps high‑tech kit running 24/7, this guide explains how to land a CMR Surgical job in 2025.