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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

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

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 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

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

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. Global Regulatory S

Senior Regulatory Affairs Contractor / Consultant. Strong focus on process development, documentation, and regulatory compliance standards. Experience supporting organisations expanding beyond the UK/EU, with awareness of broader regulatory considerations.

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

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

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.

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

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

Freyr's client is seeking a Regulatory Affairs Manager to fill a critical role in supporting development and execution of global regulatory strategies for investigational submissions, with a focus on EU and UK CTR. Provide critical support in developing global regulatory strategy, planning, and exec

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

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.

Halianis currently recruitingfor an experienced Reg affairs Risk Management specialist for a manufacturing client in theCotsworlds. Location: UK (multi-site flexibility)Industry: Medical DevicesEmployment Type: Full-time, PermanentA leading UK-based medical device manufacturer is seeking an experien

It serves as the primary point of contact for regulatory and product safety matters, supports business decisions through impact assessments, and drives harmonization of stewardship processes, SDS, labeling, and regulatory proje. This role provides product stewardship and regulatory support for the C

Senior Regulatory Affairs and QA Specialist - Medical Devices. Senior Regulatory Affairs & Quality Assurance Specialist. Biomedical Engineering, Life Sciences, Regulatory Affairs, or similar).

G&L have multiple positions available for Regulatory Affairs Manager. Regulatory Affairs within the pharmaceutical industry. Your work ensures our products continue to meet global regulatory expectations throughout their lifecycle.

A growing medical device organisation near Watford is seeking a Regulatory Affairs Manager for Class I wound-care devices. Ideal candidates have over 5 years in regulatory affairs with expertise in UKCE marking and ISO 13485. The role entails leading regulatory compliance efforts, managing Technical

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

Head of Spectrum & Regulatory Affairs. You will define and execute the regulatory and spectrum strategy required to secure and protect ITU filings, enable international market access, and ensure compliance across all operational jurisdictions. Oversee technical studies supporting regulatory submissi

This role offers the chance to work with leading banks on regulatory reforms, focusing on financial crime and compliance issues. Ideal candidates will have regulatory expertise, strong analytical skills, and experience in AML.

We’re looking to hire a Legal Counsel to join our Public Affairs & Regulatory team. Supporting the Public Affairs team on advocacy initiatives, including assisting with: consultation responses to regulators and policymakers, drafting amendments to legislative proposals, determining policy position

An international medical device company based in the United Kingdom is seeking a Director of Regulatory Affairs. The ideal candidate will possess over 15 years of experience in regulatory affairs, preferably in the medical device sector, and have proven leadership abilities across multiple countries

A leading regulatory solutions provider in the United Kingdom is seeking a Regulatory Affairs Manager to enhance quality management systems. The ideal candidate will have a Bachelor's degree, 2 years of experience in regulatory affairs, and knowledge of FDA and ISO standards. This position will ensu

A fast-growing tech company in Greater London seeks a Legal Counsel to join their Public Affairs & Regulatory team.

A leading organization in regulatory affairs is seeking a Regulatory Affairs Manager based in the United Kingdom. Responsibilities include tracking employee training, maintaining regulatory documentation, and liaising with regulatory agencies.

At least 3 years' experience in Regulatory Affairs, Clinical Regulatory, or a related discipline within the IVD, medical device, or pharmaceutical sectors. Senior Regulatory Affairs Specialist (IVDR / CDx Performance Studies). You will play a key role in shaping regulatory strategies, driving timely

For this reason, we’re looking for a Director of Regulatory Affairs to work closely with the existing regulatory team, internal and external experts, and contribute to the successful execution of our pivotal clinical program and commercialization. Maintain links with external regulatory network, p

Regulatory Affairs ManagerLondon, United Kingdom## Join UsAt Vodafone, we’re not just shaping the future of connectivity for our customers – we’re shaping the future for everyone who joins our team. Who you are*** Strong analytical capability: Demonstrated ability to develop clear, practic

Regulatory Affairs & Quality Control Executive. Quality Control and Regulatory Affairs experience preferred but not essential. Compiling Regulatory dossiers for worldwide submission and liaising with Export customers.

We are seeking an experienced Senior Regulatory Manager with strong expertise in EMA regulatory affairs to join their dynamic team. Strong regulatory affairs experience with a focus on EMA submissions. This role offers the opportunity to lead regulatory strategy, manage submissions, and act as a key

This role assists in creating, developing, and implementing global regulatory affairs procedures and educating others on global regulatory expectations and requirements. Represent Regulatory Affairs on project teams by attending team meetings and providing the required plans, procedures and regulato

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. Regulatory Affairs Manager (Wound Care). As the Regulatory Manager, you will take ownership of a

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

Strong analytical strength for establishing effective and business relevant advice in the context of sometimes ambiguous legal, regulatory and political environments.

Job Description:Job Title: Senior Manager, Regulatory Affairs CMCReports to: Executive Director, Regulatory Affairs CMCDepartment: Regulatory AffairsHours: Full timeLocation: UKAbout Autolus**Autolus is a biopharmaceutical company, advancing innovative therapies at both clinical and commercial s

Provide regulatory input on pharmaceutical development and CMC and review quality documentation to ensure regulatory compliance with UK and EU legislation. In depth knowledge of UK and European regulatory affairs legislation and guidance. Responsible for the provision of full regulatory input and su

Head of Spectrum & Regulatory Affairs. Head of Spectrum & Regulatory Affairs. Act as the key regulatory interface for Mission Operations, Ground Segment and engineering teams.

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. Understanding of current regulatory priorities across the sectors in 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

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. Head of Regulatory Affairs – UK & Ireland. Advanced qualifications such as a PhD,

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 digital finance company is seeking an experienced Head of Regulatory Affairs to design and execute global regulatory strategies for their Tether Data business. Applicants should have a strong background in regulatory affairs and excellent communication skills. This role requires expertise

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