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The Regulatory Affairs Specialist role provides. Regulatory Affairs Department,. Notified Bodies and Regulatory Agencies.

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

With expanding development programmes, evolving regulatory expectations and increased operational complexity, this is an exciting opportunity to step into a pivotal role that blends Regulatory Affairs and Quality Assurance. This position is ideal for a strong Regulatory professional with QA exposure

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

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

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. Principal / Senior Regulatory Affairs CMC Consultant. This role is with a rapidly growing international regulatory consult

You will sit within the wider Regulatory Affairs team and will work very closely with the Regulatory Affairs Director for Colonis. While the role is not primarily client-facing, you will engage directly with regulatory authorities, including participation in agency meetings The role requires someone

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. Review regulatory d

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

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.

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.

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

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.

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

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

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

Lead regulatory intelligence: scan, interpret, and brief on emerging EU/UK and market regulatory changes; maintain an actionable requirements inventory and publish timely alerts/guidance. Regulatory Affairs Product Manager – General Products & Cosmetics (EMEA). This role is part of Kimberly‑Clar

A leading pharmaceutical company in the United Kingdom is seeking a Quality Assurance Regulatory Affairs Manager to oversee compliance in regulatory affairs. This mid-senior level contract role involves collaboration with cross-functional teams to design and develop effective training concepts, esse

This role requires a qualified solicitor with significant experience in financial services and expertise in technology contracts and regulatory frameworks. A leading fintech company is seeking a Head of Legal to provide practical legal guidance and support across corporate governance, commercial con

The Regulatory Affairs Lead provides expert telecoms and digital regulatory guidance across these lines of business, and acts as a key subject‑matter expert (SME) in implementing the Group Telecom Regulatory Compliance Policy. Responsible for the delivery of telco regulatory compliance advice to t

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

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

The Head, Global Scientific and Regulatory Affairs (GSRA), Europe Middle East & Africa (EMEA) Region, is the regional lead responsible for providing leadership and direction to the scientific and regulatory function in the region. Head of Scientific and Regulatory Affairs. Vice President, Global Sci

A public health regulatory agency in Greater London seeks a Principal Policy Lead to oversee EU regulatory initiatives in medicines and medical devices.

A global pharmaceutical firm is seeking a Regulatory Affairs Manager to oversee regulatory activities across a diverse portfolio. Ideal candidates have a Life Sciences degree and experience in regulatory affairs within the pharmaceutical sector.

An established industry player is seeking a dedicated and experienced professional to lead a national approval team in the pharmaceutical sector.This role involves supervising team operations, ensuring compliance with quality standards, and fostering a collaborative environment.The ideal candidate w

Head of Regulatory Affairs, Compliance and Information Governance provides organisational leadership across regulatory compliance, information governance, clinical safety, medical device regulation, and organisational assurance frameworks. Lead the organisation’s regulatory pathway towards medical

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

The Director, Regulatory Affairs leads a team responsible for developing and executing regulatory strategies for new and revised products in global markets. Minimum 15 years in medical device regulatory affairs and quality assurance. Lead, coach, and develop a high-performing NPI Regulatory Affairs

An established industry player is seeking a Regulatory Affairs professional to join their dynamic team. In this role, you will contribute to regulatory documents and reports, manage submissions, and provide essential support to ensure compliance with EU regulations.

You’ll be the go-to expert for regulatory and sustainability issues, driving advocacy and shaping the future of coatings.

A leading review platform in the UK is seeking a Legal Counsel to join their Public Affairs & Regulatory team. The successful candidate will navigate complex regulatory environments, ensuring legal compliance and supporting various teams in understanding regulatory issues.

Arxada is seeking a Regulatory Affair Specialist accountable to the Senior Manager Regulatory Affairs for supporting the Professional Hygiene and Home Care regulatory programme. The regulatory specialist will provide a high level of expertise and guidance ensuring that the regulatory strategy for th

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

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. Director - Litigation, Competition & Regulatory Affairs, EMEA

Provide strategic and regulatory advice on CMC aspects of drug development. Develop drug development plans, gap analyses, and international regulatory strategies. Lead multi-country projects and represent clients in regulatory interactions.

A leading international telecommunications firm in London is seeking a Regulatory Affairs Manager.

A leading medical device firm in the United Kingdom is seeking a skilled Regulatory Affairs Manager. In this role, you will lead the Regulatory Affairs team and be responsible for managing registrations, certifications, and compliance. This position requires a strong background in medical device reg

A leading investment firm in London is seeking an individual to support its Public Affairs team in achieving regulatory objectives.

At least 6 years of relevant experience in a Financial Markets Front Office environment, preferably in a Market structure or Regulatory affairs role, or a hands-on, delivery-oriented Financial Markets Regulatory Legal role;. Delivering on the core regulatory expertise required of the role in accorda

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

Arxada is seeking a Regulatory Affair Specialist accountable to the Senior Manager Regulatory Affairs for supporting the Professional Hygiene and Home Care regulatory programme. Regulatory Affairs Specialist page is loaded## Regulatory Affairs Specialistlocations: UK - Manchester: PL - Warsawtim