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The Regulatory Labeling Manager: Drives and optimizes the strategy for the creation and maintenance of Core Data Sheet (CDS). Provide guidance and expertise to product teams on CDS supporting documents Authors and maintains CDS, as well as manages the CDS processes in collaboration with regulatory product responsible and product team. Drives and optimizes the strategy for the creation and maintenance of EU and US product information package. Authors and maintains these product information documents. Leads/contributes company responses to HA questions pertaining to EU and US labeling. Provides regulatory strategic recommendations concerning acceptable labeling in regional markets, in collaboration with the relevant functions. Guides and supports the implementation of CDS into the Local Product Labels and manages local label deviations. Gives specific guidance on labelling regulatory issues such as legislation, guidelines, procedures to the RAFT and Project teams. Leads or contributes to establishment or improvement of working processes and standards Do you hold experience in CCDS/ CDS/ Cored Data Sheets?

Benefits: 12-month contract outside IR35 Hybrid working with flexibility for remote working Opportunity to work on global regulatory strategy Collaborative cross-functional environment The Requirements: Degree in Life Sciences or a related field Strong experience within regulatory affairs, ideal

Join Our Team as a Regulatory Labeling Manager! Are you passionate about regulatory affairs in the pharmaceutical industry? Do you have a knack for strategic labeling and a desire to make a meaningful impact on product lifecycle management? If so, we have an exciting opportunity for you! Position:

A global healthcare company is seeking a Regulatory Affairs Executive in Hatfield, England, on a fixed-term contract.The role focuses on regulatory activities such as rebranding and labelling updates across the EU and UK.Candidates should have a strong understanding of European regulatory affairs an

The ideal candidate will author and maintain CDS and product information documents while providing strategic recommendations for labeling. The position offers a collaborative environment with product teams to enhance labeling compliance.

A leading pharmaceutical organization based in Hatfield, UK, is seeking an Associate Director of Regulatory Affairs to oversee regulatory activities for its Neurology product portfolio.

Ein führendes Pharmakonzern in Hatfield sucht einen Regulatory Affairs Executive für ein 12-monatiges befristetes Arbeitsverhältnis. Anforderungen sind unter anderem Kenntnisse im europäischen Regulatory Affairs und Erfahrung mit MHRA-Anträgen.

Regulatory Affairs Executive (12 Month Fixed Term Contract) page is loaded## Regulatory Affairs Executive (12 Month Fixed Term Contract)locations: Hatfield, England, United Kingdomtime type: Vollzeitposted on: Heute ausgeschriebenjob requisition id: R5666234Generics [U.Bei VIATRIS, sehen wir

Talentmark are recruiting for a Regulatory Labelling Manager to join a company in the pharmaceutical industry on a contract basis for 12 months. Salary: £65 – £70 per hour (Outside IR35) Regulatory Labelling Manager Role: Drive and optimise regulatory labelling strategy across the full product lifecycle. Author, maintain, and manage Core Data Sheets (CDS) and associated documentation. Lead the development and maintenance of EU and US product labelling. Provide strategic regulatory input on labelling requirements across global markets. Support product teams with CDS implementation and manage local label deviations. Respond to Health Authority queries related to labelling. Collaborate cross-functionally with regulatory, product, and project teams. Contribute to continuous improvement of labelling processes and standards.Your Background: Degree in Life Sciences or a related field. Strong experience within Regulatory Affairs, ideally with a focus on labelling strategy. Proven experience working with CDS and global labelling documentation. Knowledge of market access considerations is advantageous.Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Location: This role is based at our clients site in Welwyn Garden City (Hybrid – 1 to 2 days on site). Apply: For more information, or to apply for this Regulatory Labelling Manager role please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (phone number removed) / 40038. It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check

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

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 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

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

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

Senior Regulatory Affairs Contractor / Consultant. Broad exposure to end to end LCM across Europe, ranging from artwork implementation through to regulatory strategy. Strong focus on process development, documentation, and regulatory compliance standards.

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

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

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

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

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

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

An interest in politics and current affairs, keeping your finger on the pulse of the regulatory environment. 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 respon

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.

Biomedical Engineering, Life Sciences, Regulatory Affairs, or similar). Minimum of 2 years' experience in a Senior Quality Assurance & Regulatory Affairs position within the medical device industry. Senior Regulatory Affairs and QA Specialist - Medical Devices.

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.

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

A growing medical device organization is looking for an experienced Regulatory Manager to oversee regulatory operations for Class I medical devices. Candidates should have 5+ years of experience in regulatory affairs specific to medical devices and must work on-site in Watford. This position offers

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 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.

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. You will handle a wide range of litigation matters, working c

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

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 global entertainment leader is seeking a Director for Litigation, Competition & Regulatory Affairs for the EMEA region. Candidates must possess a Juris Doctorate, experience in regulatory compliance, and exhibit strong communication and decision-making skills.

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 be followed and implemented. Vice President Scientific Affairs and Regulat

Quality Assurance Regulatory Affairs Manager.

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

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

You will provide high-quality regulatory advice on human medicinal products and support product development. Provide strategic and regulatory advice on CMC aspects of drug development. Minimum 5 years of regulatory experience (FDA, EMA, MHRA or national authority).

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.

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

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.