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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 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

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

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

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

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

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

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.

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.

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’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

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 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

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

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

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

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

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

Manager Regulatory Affairs #J-18808-Ljbffr. 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: De

Demonstrated practical experience in digital device regulatory affairs (e. Author and/or review compliant digital device documentation for Health Authority submissions, applying agreed digital device global regulatory strategies, current regulatory standards and guidelines. Experience leading regula

Strong knowledge of regulatory affairs, particularly in strategic labeling; familiarity with market access is a plus. Keep the heartbeat of innovation running and join our client in this Regulatory Affairs Labelling position and ensure cutting-edge pharma operations never miss a beat!. Proclinical i

A global entertainment leader is seeking a Director for Litigation, Competition & Regulatory Affairs in the EMEA region. The role involves advising on litigation and regulatory matters, representing the company before authorities, and ensuring compliance with laws. Candidates should possess a Juris

A leading pharmaceutical organization is seeking a Regulatory Affairs Manager to support product development and lifecycle activities. The role involves leading EU regulatory submissions, contributing to clinical regulatory strategies, and ensuring compliance.

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

A clinical-stage biopharmaceutical firm in the United Kingdom is seeking a Director, Regulatory Affairs CMC. The successful candidate will leverage a minimum of 10 years of experience in Regulatory Affairs, involving detailed knowledge of large molecule biologics and FDA/EU regulations. This leaders

The ideal candidate should have a degree in a scientific field and substantial experience in regulatory affairs. A recruitment agency in pharmaceuticals is seeking a professional for a mid-senior level role focusing on regulatory input for product submissions. You will manage complex regulatory subm

Lead and inspire our Regulatory Affairs team, helping everyone thrive while managing registrations, certifications, and compliance. Experience in medical device regulatory affairs (MDD, MDR, IVDD, IVDR, UK MDR, ISO 13485). Are you passionate about regulatory affairs and want to play a key role in br

A leading telecommunications company is seeking a Regulatory Affairs Lead in Greater London.

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. Policy Advocacy, Monitoring, Analysis and Guidance: Monitor, analyse and communicate changes in global regulatory policies, and

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

We are looking to hire a Legal Counsel to join our Public Affairs & Regulatory team. An interest in politics and current affairs, keeping informed about the regulatory environment. Your primary focus will be to help maintain Trustpilots reputation as a trusted and compliant platform by navigating a

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

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 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

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.

Quality Assurance Regulatory Affairs Manager.

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

Vice President Scientific Affairs and Regulatory Engagement, Switzerland. Crucial to your success will be your ability to work closely with the FDA and other regulatory bodies to agree innovative scientific approaches and provide the internal leadership to convert this into a regulatory strategy to

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

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

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

A leading pharmaceutical company in the United Kingdom is seeking a Mid-Senior level Regulatory Affairs Specialist to provide regulatory input and support for new Marketing Authorisation Applications. The ideal candidate will have a strong background in regulatory submissions and CMC, with an emphas

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.

A leading nutritional health company is seeking a Regulatory Affairs & Quality Control Executive to join their Technical & Quality Control Department. Key responsibilities include compiling regulatory dossiers and managing product development.