regulatory affairs assistant jobs in Leeds, West Yorkshire

You will receive full training in order to provide support to the regulatory affairs department.

You will have a science-based degree and be looking for a starting role in regulatory affairs – you must enjoy working for a multi-skilled, busy team working in a global environment.

You will receive full training in order to provide support to the regulatory affairs department.

You will have a science-based degree and be looking for a starting role in regulatory affairs – you must enjoy working for a multi-skilled, busy team working in a global environment.

Senior Regional Regulatory Affairs Lead - Oncology (EU Markets) Your new company Are you a seasoned regulatory affairs professional with a passion for oncology and a deep understanding of European regulatory frameworks? Our client, a leading global biopharmaceutical company, is seeking a Senior Regional Regulatory Affairs Lead to drive regulatory strategy and execution across the EU region for...

You must be looking to use your degree in a desk-based role and be interested in regulations and compliance. Strong attention to detail is an absolute must have.

Regulatory Affairs Specialist (UK Market) – Remote (Part-Time or Full-Time) Contract Type: 12-month contract (possibility of extension) Workload: Part-time (20h/week) or Full-time Location: Remote (within Europe) Start Date: ASAP About the Role We are seeking an experienced Regulatory Affairs Manager with strong UK market experience to support ongoing regulatory activities across the UK and...

About Freyr Freyr is a fast-growing, innovative company specializing in providing end-to-end regulatory solutions and services for the Life Sciences industry. With a commitment to excellence and innovation, we assist pharmaceutical, medical device, and biotech companies in navigating the complexities of regulatory compliance. Why Freyr? At Freyr, we believe in fostering a collaborative and...

Job Title: Department Leader – Regulatory Affairs– IVD’s Job Type: Full-Time, permanent position Location: Outskirts of Edinburgh, Scotland, UK – 3x a week on site or REMOTE with ocassional travel once per month Remuneration: Competative remuneration package The role is a full-time, permanent position working 37.5 hours per week. Reporting into the Head of Quality and Regulatory Affairs. This...

We are supporting a pharmaceutical company committed to delivering innovative therapies that improve patients’ lives in recruiting a Senior Regulatory Manager. Their global teams collaborate to bring cutting-edge solutions from concept to market while maintaining the highest standards of quality and compliance. The Role: We are seeking an experienced Senior Regulatory Manager with strong...

Are you an expert in chemical regulation with a passion for guiding companies through complex compliance landscapes? Do you have management experience, a consultancy background, and want to evolve in a leading Regulatory function? We’re recruiting on behalf of a leading global consultancy working at the cutting edge of chemical and environmental regulation! With offices across Europe and North...

Senior Consultant, Medical Affairs Strategy We're seeking a strategic and forward-thinking Senior Consultant to join a top medical communications agency within their Medical Affairs Strategic Advisory team. In this role, you'll lead the design and execution of omnichannel engagement strategies that support Medical Affairs objectives across the entire product lifecycle - with a strong focus on...

SmartSearch's distinctive Anti-Money Laundering verification software protects our clients by offering the most advanced and comprehensive features available from an AML provider. SmartSearch has grown rapidly by fostering an incredibly collaborative and supportive culture. As we continue our ambitious growth plans, we will strive to remain a truly exciting, rewarding, and unique place to...

PRINCIPAL CHEMICAL REGULATORY CONSULTANT Location: Remote - UK or Ireland I am representing a respected regulatory consultancy that supports chemical and life-science companies with compliance across REACH, CLP, BPR, and GHS. The organisation has grown rapidly in recent years, known for combining technical depth with commercial understanding. However, they were also one of the key founding...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare...

COMPLIANCE & SDS MANAGER – CHEMICAL COMPLIANCE AND/OR SAFETY DATA EXPERIENCE FROM CHEMICALS OR MANUFACTURING REQUIRED £50K - £55K + Benefits (inc Car) & Bonus Hybrid (North or South Yorkshire) Our client, a leading chemicals firms, seeks a Compliance / SDS Manager to be responsible for managing the creation, distribution, and compliance of Safety Data Sheets (SDS) for their products. Develop,...

Complete Regulatory is part of IPG Health Medical Communications, home to the world’s most awarded and celebrated Med Comms agencies. With over 800 dedicated experts, we combine science, creativity, and technology to craft exceptional medical communications solutions for leading pharmaceutical companies worldwide. What We Do We specialize in regulatory writing and consultancy services,...

Who are we? Howden is a collective – a group of talented and passionate people all around the world. Together, we have pushed the boundaries of insurance. We are united by a shared passion and no-limits mindset, and our strength lies in our ability to collaborate as a powerful international team comprised of over 20,000 employees spanning more than 100 countries. We're moving from strength to...

You will work closely with Public Affairs Lead to deliver and execute the public affairs strategy for the region.

You should be skilled at stakeholder engagement, building relationships with government, Parliament, regulators, think tanks, Combined Authorities, and other influential groups, providing strategic and tactical advice as needed.

An innovative biopharmaceutical company is seeking a EU Medical Affairs Director to lead its neurology portfolio through upcoming product launches across Europe. This is a fully remote position, offering strategic oversight and team leadership within a fast-growing organisation. Key Responsibilities: - Lead medical strategy and launch readiness for neurology products across EU markets. - Manage...

You will also be responsible for safeguarding client data and ensuring compliance with regulatory standards. What you'll need to succeed To be successful in this role you will need: - Strong communication and client-facing skills - A good working knowledge of the UK self-assessment tax system

You must be looking to use your degree in a desk-based role and be interested in regulations and compliance. Strong attention to detail is an absolute must have.