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MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across global development and lifecycle activities within a leading pharmaceutical organisation. Lead and support planning, coordination, and preparation of EU regulatory submissions. Contribute to EU cl

Senior Regulatory Affairs Manager – Europe. Support regulatory interactions, including scientific advice and dossier due diligence (Modules 1–5). Hands on, proactive regulatory with authoring and submission experience.

Pennaeth Polisi RheoleiddioCasnewydd, Cymru (gyda gweithio Hybrid)Amdanom NiNi yw Cymwysterau Cymru, y sefydliad annibynnol sy'n gyfrifol am reoleiddio cymwysterau cyffredinol a galwedigaethol yng Nghymru.Ein blaenoriaethau strategol dros y pum mlynedd nesaf yw:- Datblygu ystod gydlynol a chynhwysol

Liaise with local Regulatory Affairs staff on regulatory documentation, including labelling, variations, and new registrations. We’re looking for an experienced Regulatory Manager to execute activities across international markets and EMEA. Lead dossier remediation activities, such as aligning old

Our Regulatory team is looking to recruit experienced full-time advocates with extensive trial advocacy experience to respond to increasing volumes of work and new client wins.

PermanentFull-time (37 hours per week)Flexible working options (including hybrid)About the roleAn exciting opportunity has arisen for a Lawyer in the Legal Shared Service Litigation and Regulatory team. This pivotal role will predominantly: Support the Litigation and Regulatory team Provide the deli

With a strong focus on advanced polymer science, regulatory compliance, and quality excellence, they support a growing customer base across food-contact and performance-critical applications.

MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across global development and lifecycle activities within a leading pharmaceutical organisation. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

Global payments and digital assets company is seeking a regulatory lawyer (3+ PQE) as part of their expansion plans. Our client is seeking a lawyer either from private practice or in-house to support them on a broad range of regulatory matters.

CMC regulatory strategy across development and lifecycle programs. CMC regulatory documentation and CTD Module 3. CMC development and regulatory submissions.

Research and apply regulatory intelligence and knowledge of strategic options to enable innovative regulatory pathways and solutions for complex global requirements and regulatory challenges. Provide critical support in developing global regulatory strategy, planning, and execution of global investi

Regulatory CMC Technical Writer. Regulatory CMC Technical Writer. Translate complex scientific, manufacturing, and quality information into clear, compliant regulatory content.

This is a global-facing role responsible for advising on a wide range of regulatory matters across multiple jurisdictions, including licensing and registration applications, and regulatory engagement. Lead and support regulatory license and registration applications globally, including supporting Le

Regulatory processes, systems, optimisation, upgrade, regulatory developments, functionality implementations, user training, SAP, SAP S4 HANA, legacy SAP systems, regulatory affairs, product stewardship. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product

We're looking for an experienced Regulatory Affairs Manager to focus on financial crime related regulatory engagements, ensuring communication with external regulators is transparent, compliant, and efficient. Expertise in the UK FinCrime regulatory environment. Familiarity with key regulatory compl

Title : Regulatory Affairs Associate - Regulatory Operations - Publishing. Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. We partner with leading pharmaceutical, biotechnology, and medic

Own regulatory reporting & notifications (incl. Advise on UK regulatory requirements (FCA Handbook etc). You will be an experienced compliance professional within UK regulated financial services and you will have a strong working knowledge of the UK regulatory framework.

The Regulatory Affairs Specialist reports into RA leadership and is responsible for regulatory compliance, regulatory submissions, and supporting regulatory planning and execution across the organisation. You will be involved in preparing and reviewing regulatory submissions, maintaining technical d

As a key member of the Regulatory Affairs CMC team, the candidate will have responsibility for developing CMC regulatory strategy for the clinical portfolio from a Regulatory CMC perspective and for communicating critical issues to Senior Management. To lead meetings with Health Authorities in conne

I’m working with a major infrastructure organisation looking to bring in a senior hire to take ownership of water quality and regulatory compliance across multiple regions. Leading monitoring strategies, sampling programmes, and regulatory compliance.

Regulatory Operations / eCTD publishing. Manager, Regulatory Operations (eCTD Publishing). A clinical-stage biotech is expanding its EU team following significant growth and is looking to hire a Manager, Regulatory Operations to support global submissions across a robust oncology pipeline.

Define and oversee regulatory strategies for submissions to the Medicines and Healthcare products Regulatory Agency (MHRA) and other relevant authorities. Influence regulatory policy and stakeholder relationships to support market access, innovation and long term growth. Partner with cross functiona

Are you an experienced regulatory professional looking to shape global strategy and influence product development at an international level? This is an exciting opportunity to a global Pharmaceutical Manufacturing organisation as an Associate Director, Global Regulatory Strategy. Author Scientific A

To be successful as the new Quality Assurance & Regulatory Affairs Administrator, you will bring strong administrative experience with excellent attention to detail and a methodical approach to document creation. Experience within a regulated environment such as medical devices or pharmaceuticals wo

Contribute to onboarding and training of new regulatory writers. Associate Director, Regulatory Writing. Lead the development of high-quality regulatory documentation, ensuring outputs meet or exceed client expectations, are delivered on time and within budget, and provide meaningful value to client

You’ll have the opportunity to specialise within regulatory writing while also expanding your knowledge across strategic submissions, global regulatory pathways, and therapeutic areas—within a truly one-of-a-kind regulatory offering. Omnicom Health Regulatory is a global, market-leading regulato

Senior Regulatory Affairs Contractor / Consultant. Strong technical regulatory experience, particularly in Lifecycle Management (LCM). Broad exposure to end to end LCM across Europe, ranging from artwork implementation through to regulatory strategy.

You’ll have the opportunity to specialise within regulatory writing while also expanding your knowledge across strategic submissions, global regulatory pathways, and therapeutic areas—within a truly one-of-a-kind regulatory offering. Demonstrate a good understanding of the needs of regulatory au

As a Principal or Senior Regulatory Affairs CMC Consultant, you will play a key leadership role, providing high-level regulatory and technical guidance for complex therapeutics. This role is with a rapidly growing international regulatory consulting organization focused on advancing healthcare innov

We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors. REACH, EU REACH, UK REACH, Turkey KKDIK,

You’ll have the opportunity to specialise within regulatory writing while also expanding your knowledge across strategic submissions, global regulatory pathways, and therapeutic areas—within a truly one-of-a-kind regulatory offering. Omnicom Health Regulatory is a global, market-leading regulato

This role suits experienced regulatory professionals. Support regulatory capability and process development. Experience in Regulatory Affairs within the pharmaceutical industry.

Due to company growth and expansion into new territories, they are now looking for a Global Regulatory Technologist to join the team. Develop and implement regulatory strategies to support the successful launch products in global markets. Support internal and external teams with regulatory queries.

I am partnered with a growing, high-performing regulatory and medical communications organisation to appoint an experienced Regulatory Writing leader at the Associate Director, Director, or VP level. This is a key leadership role combining hands-on regulatory writing, team leadership, and strategic

You'll be making regulatory strategy decisions with direct commercial consequences — classification rationale, predicate selection, clinical evidence sufficiency, post-market surveillance design, and regulatory timing relative to commercial milestones. We need a regulatory affairs professional who

Lead the development of clear, concise, and scientifically accurate regulatory documentation, ensuring appropriate interpretation of data. Apply strong knowledge of regulatory authority requirements to inform document strategy and provide guidance to clients and internal teams. Deliver high-quality

Depth of regulatory experience enabling the creation of effective regulatory strategies and innovative approval pathways. As Regulatory Affairs Manager, you will define and deliver UK/EU regulatory strategy across a diverse portfolio of products, including a significant new Class III device developm

Provide oversight of high-quality submissions to regulatory authorities, including the Medicines and Healthcare products Regulatory Agency (MHRA). Our client is seeking a strategic leader to define and execute regulatory strategy while leading a high-performing Regulatory Affairs function. Maintain

A rapidly growing, clinical-stage biotech is expanding its European Regulatory team and is looking to appoint an Associate Director, Regulatory Affairs to support global Oncology development programs, with a focus on EU strategy and submissions. Strong experience with EU regulatory submissions (CTA/

Around 3+ years in a chemical regulatory role. You can explain regulation to non-regulatory people (this matters more than people admit). You’ll influence regulatory direction, not just follow it.

Location: UK (multi-site flexibility)Industry: Medical DevicesEmployment Type: Full-time, PermanentA leading UK-based medical device manufacturer is seeking an experienced Risk Management Specialist to join its Quality & Regulatory team.

This role of Permitting & Regulatory Specialist is to ensure we are compliant with the reporting requirements of our Environmental permits and to submit the necessary regulatory reports to the regulator so our environmental performance can be assessed. It will work alongside existing roles that fulf

What you’ll be doing as a Regulatory Enforcement AdvisorIn this role, you will respond to Environment Agency (EA) formal requests for information as part of a criminal investigation within the regulatory deadline via written correspondence. Regulatory Enforcement Advisor - Reading, Berkshire, RG1

Costing of capital analysis, including considering the regulatory perspective and future projections of financing costs. Led strategic creative thinking around ensuring the development of future regulatory approaches is best aligned with the requirements of our customers and shareholders. What you s