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This role provides product stewardship and regulatory support for the CBG and EPS businesses across the EMEAI region, ensuring compliance with consumer product regulations.It serves as the primary point of contact for regulatory and product safety matters, supports business decisions through impact

The Senior Manager QRA UKI and Nordics leads the Quality Assurance and Regulatory Affairs function across the region, ensuring full compliance with internal standards and external regulatory requirements. Strong experience in Regulatory Affairs management with proven expertise in compliance and regu

Represents the Regulatory Affairs function as appropriate in Cluster and EMEA Regulatory Affairs Leadership teams. The Director of Regulatory Affairs has an in-depth understanding of the regulatory environment within their geographical area of responsibility as well as requirements and strategies fo

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Regulatory Affairs Manager (EU) | Leading Pharma. MAA, contributing to EU regional clinical regulatory st

The intern will be assigned to the UK or EMEA Regulatory Affairs department and will work with a range of projects for the duration of the term. Works to provide regulatory input and technical guidance on local regulatory requirements to product development teams. Provides regulatory assessment and

Pharmaceuticals Regulatory Affairs Associate – Homebased and Office Opportunity: This is a great opportunity for a Regulatory Affairs (RA) Specialist to develop your career in regulatory affairs for drug products. Your role as a Pharmaceuticals Regulatory Affairs Associate will involve suppo

Regulatory Affairs Department,. The Regulatory Affairs Specialist role provides.

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across g

You’ve built experience in a regulatory or quality-focused admin role, and you take pride in keeping things accurate, organised, and audit-ready. You’ll support the quality and regulatory teams with keeping their processes and procedure in good shape. Ensuring processes related to quality/regula

Strong experience within Regulatory affairs. A Pharmaceutical company in Berkshire are seeking a Regulatory Affairs Officer to join their team. Create and maintain SOPs and Work Instructions for the Regulatory team.

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

You will lead the UK & Ireland Regulatory Affairs team and act as the primary liaison with Health Authorities, ensuring regulatory compliance and excellence across both markets. As the Senior Regulatory Affairs Manager, you will be accountable for providing regulatory leadership, strategy, and opera

Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. Research and apply regulatory intelligence and knowledge of strategic options to enable innovative regulatory pathways and solutions for co

UK + Ireland Regulatory Affairs Officer. UK + Ireland market experience in Regulatory Affairs. Previous experience in Regulatory Affairs within the pharmaceutical industry.

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. Represent clients in interactions with regulatory agencies and provide solutions to regulatory challenges and objections.

You will oversee regulatory project management and act as a key partner to global Regulatory Affairs teams, R&D, Clinical Affairs, and wider cross‑functional groups. As Regulatory Affairs Manager, you will define and deliver UK/EU regulatory strategy across a diverse portfolio of products, includi

You will sit within the wider Regulatory Affairs team and will work very closely with the Regulatory Affairs Director for Colonis. This is a dedicated Regulatory Affairs Manager role supporting Colonis, a Clinigen Group company. To support our growth, we are seeking a dynamic, detail orientated and

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. Provide strategic i

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.

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. Experience 2 to 5 years in Regulatory Affairs.

Associate Director – Regulatory Affairs CMC. CMC development and regulatory submissions. EU and/or US CMC regulatory requirements and ICH guidelines.

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. The Regulatory Affairs team builds transparent relationships with regulators to keep Revol

We are working with a leading pharmaceutical company who are seeking an experienced Senior Manager, Regulatory Affairs to shape and drive regulatory strategy across the Europe Area. Senior Manager, Regulatory Affairs (Consultant). Collaborate with affiliate Regulatory Affairs teams to guide submissi

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. We are seeking a Regulatory Affairs Specialist with hands-on experience in software medical dev

The successful candidate will be responsible for leading regulatory activities for international projects, providing regulatory guidance and liaising with external partners including regulatory authorities. Prior US medicinal regulatory affairs experience and familiarity with global regulations, inc

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. Halianis currently recruitingfor an experienced Reg affairs Ri

Provide ongoing regulatory support to the regulatory affairs team lead and project teams to ensure regulatory concerns are addressed and relevant data is generated to meet project objectives. Contribute to regulatory documents and reports for regulatory submission. Document and track regulatory subm

Strong communication and coordination skills in order to achieve a consistent approach to engaging with the regulators in the UK and as necessary across the EMEA Division including the preparation and/or review of regulatory communications, briefing of senior management, including Board and Manageme

We are working with a leading pharmaceutical company who are seeking an experienced Senior Manager, Regulatory Affairs to shape and drive regulatory strategy across the Europe Area. Senior Manager, Regulatory Affairs (Consultant). Represent regional regulatory requirements within global regulatory p

We’re looking for a Regulatory Affairs Consultant to help us shape and deliver our regulatory strategy across the Group. Coordinating responses to regulatory consultations and analysing publications from key regulatory bodies. Maintaining positive and transparent relationships with the PRA and FCA

A major financial institution is seeking a Head of Regulatory Affairs for a 12-month fixed term contract. The ideal candidate will have strong knowledge of the PRA and FCA, excellent communication skills, and experience in regulatory affairs. The role involves leading regulatory engagement with UK r

With an expanding product portfolio and a commitment to quality, safety, and regulatory excellence, the business is seeking an experienced Regulatory Manager to lead and strengthen regulatory operations. As the Regulatory Manager, you will take ownership of all regulatory activities for a range of C

As Head of Regulatory Affairs for the UK and Ireland, you will play a pivotal role on the Leadership Team, shaping and executing bold, forward-looking regulatory strategies across the entire pharmaceutical portfolio. Vast experience in the life sciences and/or pharmaceutical industry, focused to Reg

The ideal candidate will have at least 8 years of experience in regulatory affairs within biotech and expertise in clinical trial applications and international regulatory dossier preparation. A leading biotech firm in the UK is seeking a Regulatory Affairs Director to transform the treatment of neu

This is an excellent opportunity to work in chemical regulatory affairs, working with innovative product solutions and gaining hands‑on experience with raw material data management. As a Scientific Data & Regulatory Associate, you will support the technical aspects of managing raw material data wh

A leading regulatory consulting firm in the United Kingdom seeks a motivated Senior Consultant. You will provide high-quality regulatory advice on human medicinal products, lead multi-country projects, and mentor team members. The position requires at least 5 years of drug development and regulatory

A prominent pharmaceutical company in the United Kingdom seeks a Regulatory Affairs Specialist to provide full regulatory support for products. The ideal candidate will have significant experience across the product lifecycle, particularly with CMC regulatory submissions.

Tether is seeking an experienced and visionary Head of Regulatory Affairs to design and execute global regulatory affairs strategies for our Tether Data business vertical. Expertise in preparing complex regulatory documents and other major regulatory submissions, including the preparation and execut

As Director, Litigation, Competition & Regulatory Affairs, EMEA, you will be the primary litigation, competition and regulatory counsel for the Sony Interactive Entertainment (SIE) business in the EMEA region, including Europe and the UK. You will handle a wide range of litigation matters, working c

Maintain and organize regulatory documentation including job descriptions and resumes regulatory submissions correspondence with regulatory agencies and regulatory tracking databases. Collaborate with regulatory affairs teams to ensure alignment of training programs with current regulatory expectati

This role is part of Kimberly‑Clark’s Global Regulatory Affairs team enabling safe, compliant innovation across EM Europe. Regulatory Affairs experience in cosmetics and/or consumer/general products and/or BPR across EU/UK,. Regulatory Affairs Product Manager – General Products & Cosmetics –

A leading employment agency is looking for a Senior Regulatory Affairs Specialist to lead high-impact regulatory activities for IVDR Companion Diagnostics. This remote or hybrid role requires expertise in EU submissions and at least 3 years' experience in Regulatory Affairs. The successful candidate

A leading life sciences recruiter in the UK is seeking an experienced Regulatory Affairs Manager to lead a new regulatory team and ensure compliance within the pharmaceutical industry. The ideal candidate will have at least 5 years of experience and a strong understanding of regulatory processes.

A leading health and beauty company is seeking a Senior Regulatory Affairs Specialist to develop regulatory strategies across the EMEA region. Candidates should have a relevant Bachelor's Degree, expertise in regulatory classifications, and strong communication skills. The role includes evaluating r

A biotech company in Greater London is seeking a Senior Manager for Regulatory Affairs CMC. Candidates should have experience in Regulatory Affairs with a focus on biologics and strong communication and project management skills.