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As Senior Director, Regulatory Affairs, EMEA Defense Lead, you’ll join an EMEA-based team addressing the highest and emerging risks pertaining to all aspects of our business in EMEA including our people, our products, our users, legislators and society, and our ecosystem. Senior Director, Regulat...

No less than 3 years’ experience in regulatory affairs, policy, energy markets, or related commercial environments. The role focuses on anticipating and influencing regulatory developments, supporting business decisions, and building relationships with key stakeholders and regulatory bodies. Infl...

As their Regulatory Engineer, you will be responsible for managing regulatory activities, ensuring compliance with ISO 13485, EU MDR, and FDA requirements, and compiling technical documentation for regulatory submissions. Proven experience in Regulatory Affairs in Medical Devices. Cure Talent is ...

The successful candidate will be part of a global regulatory affairs team, overseeing the preparation, submission, and review of regulatory applications for health authorities across Europe and beyond. Director of Regulatory Affairs. At least 8 years of experience in the biotech or pharmaceutical...

Establish regulatory priorities and coordinate with Regulatory Affairs consultants, Quality, Manufacturing, Science & Technical (MSAT), Pharmacovigilance, and Medical Affairs teams to drive effective submission, approval, and implementation processes for the product range. As Regulatory Affairs

Proven experience in CMC regulatory affairs within the pharmaceutical or biotechnology industry. My Client is seeking a highly experienced professional to lead and optimize Chemistry, Manufacturing, and Controls (CMC) regulatory processes and systems. Ensure compliance with current regulatory gui...

They develop and deliver life-changing treatments and are seeking a Regulatory Affairs Manager on an Interim Basis to join a growing RA function. Senior Manager, Global Regulatory Affairs. This role is crucial in ensuring the company's products meet regulatory requirements for approval and contin...

As their Regulatory Engineer, you will be responsible for managing regulatory activities, ensuring compliance with ISO 13485, EU MDR, and FDA requirements, and compiling technical documentation for regulatory submissions. This newly created role is key to ensuring the successful regulatory approv...

Knowledge of regulatory intelligence sources to provide accurate regulatory advice. University degree (MSc) in life-science (pharmacy, molecular biology, regulatory affairs and/or PhD. The Senior Director, Regulatory Affairs is integral to designing and advancing the company’s effort to discover,...

Regulatory Affairs Associate - Devon -Up to £40,000 pa + benefits - Ref 1894. I am currently recruiting for a Regulatory Affairs Associate to work for a multi-national medical device organisation. This is a fantastic opportunity for a Regulatory Affairs Associate to work for a leader within their...

Senior Manager in Global Regulatory Affairs. Global Regulatory Affairs (GRA) team. Significant experience in the pharmaceutical industry, including 5+ years in Regulatory Affairs.

Regulatory Affairs Associate - Devon -Up to £40,000 pa + benefits - Ref 1894. I am currently recruiting for a Regulatory Affairs Associate to work for a multi-national medical device organisation. This is a fantastic opportunity for a Regulatory Affairs Associate to work for a leader within their...

Serve as the primary regulatory interface across internal functions and regulatory authorities. Senior Manager, Global Regulatory Affairs. Global Regulatory Affairs (GRA) team.

Regulatory and/or non-Regulatory systems that are critical for Regulatory submission and maintenance activities. Regulatory Affairs Manager - Global Clinical Trials. As the only Regulatory Affairs professional based in the UK, you must be confident with global clinical trial regulations and have ...

Regulatory Affairs Manager - Global Clinical Trials. As the only Regulatory Affairs professional based in the UK, you must be confident with global clinical trial regulations and have supported decentralised late-stage trials. Regulatory submission preparation and processing of amendments.

Regulatory Affairs Associate - Devon -Up to £40,000 pa + benefits - Ref 1894. I am currently recruiting for a Regulatory Affairs Associate to work for a multi-national medical device organisation. This is a fantastic opportunity for a Regulatory Affairs Associate to work for a leader within their...

This rapidly growing Regulatory Affairs consultancy is looking for an experienced Regulatory Affairs Manager who specialises in UK and Ire registrations to fulfil a 12-month, remote contract which is outside IR35. As Regulatory Affairs Manager UK and Ire you will be responsible for submitting reg...

Regulatory Communications Specialist - Europe, Kuiper Global Service Compliance External Affairs. The Regulatory Communications Specialist - Europe will be the external point of contact for Project Kuiper’s service compliance obligation deliverables in front of European communications regulators ...

An innovative biotech company focused on individualized genetic medicines is seeking an SVP/VP of Regulatory to lead its global regulatory strategy. Extensive regulatory affairs experience in the UK, EU, and EMEA regions. Drive interactions with regulatory authorities (MHRA, EMA, FDA) to ensure s...

This role involves working within a global regulatory affairs team, overseeing the planning, preparation, review, and submission of regulatory applications to health authorities both in Europe and internationally. With a growing regulatory team, an exciting opportunity has emerged for a Manager, ...

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Planet Pharma are working alongside a Global Biotech who are seeking 4x Regulatory Project Manager.

Tether is seeking an experienced and visionary Head of Regulatory Affairs to design and execute global regulatory strategies for our Tether Data business vertical. Head of Regulatory Affairs - AI & P2P (100% remote - UK), London. Monitor, analyse and communicate changes in global regulatory polic...

This is a fantastic opportunity for a Regulatory Affairs Associate to work for a leader within their field where the work is continuously varied keeping you engaged and challenged. Regulatory Affairs Associate - Devon -Up to £40,000 pa + benefits - Ref 1894. I am currently recruiting for a Regula...

Regulatory Affairs for Central Europe Senior Manager, London. Senior) Manager, Regulatory Affairs for Central Europe. Provides strategic Regulatory planning and vision for Avon’s Central European markets, providing leadership and strategic direction to the Regulatory teams based in Ukraine, Kyrgy...

This role is an opportunity to support a global information management team and international regulatory functions to execute business processes to a high standard, and to ensure the integrity of data used internally for business intelligence/reporting purposes and externally to comply with globa...

Support the CECO in managing global public policy and regulatory affairs strategy through the GCE Regulatory Affairs Forum, with an eye towards integration of strategies globally. The Director, Public Policy and Regulatory Affairs – Europe is responsible for systematically monitoring policy, legi...

As their Regulatory Engineer, you will be responsible for managing regulatory activities, ensuring compliance with ISO 13485, EU MDR, and FDA requirements, and compiling technical documentation for regulatory submissions. Proven experience in Regulatory Affairs in Medical Devices. This newly crea...

Expertise in preparing complex regulatory documents and other major regulatory submissions, including the preparation and execution of interactions with regulatory authorities. Tether is seeking an experienced and visionary Head of Regulatory Affairs to design and execute global regulatory strate...

Proven experience in CMC regulatory affairs within the pharmaceutical or biotechnology industry. Continuously improve CMC regulatory processes and systems to enhance efficiency and effectiveness. Ensure compliance with current regulatory guidelines and standards.

Under general supervision, implement product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements. You will be joining the European General Medicine Regulatory team, part of the Global Regulatory Affa...

Regulatory Affairs Manager – Clinical TrialsLondon | Fixed-Term (2–3 Years) | £52,000–£60,000 | Full-timeThe RoleAre you confident navigating complex global clinical trial regulations? Do you bring experience guiding research teams through the challenges of compliance in an evolving regulato

Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various European locations. As the CMC Regulatory Manager, you will play a vital role in our company's worldwide post-approval regulatory activities, specifical...

As Regulatory Affairs Advisor for one of their flagship European projects, you'll support the leadership team with expert guidance on regulatory developments affecting German and wider EU energy markets. If you are a regulatory affairs professional eager to shape the future of energy markets in G...

A Regulatory expert with a minimum of 10 years of experience in a technical/regulatory affairs role, or in a related field in one of the following markets: Germany, France, Spain, Netherlands or Belgium. If this Head of Regulatory Affairs role is of interest and you would like to investigate this...

Regulatory Affairs Associate - Devon -Up to £40,000 pa + benefits - Ref 1894. I am currently recruiting for a Regulatory Affairs Associate to work for a multi-national medical device organisation. This is a fantastic opportunity for a Regulatory Affairs Associate to work for a leader within their...

Vice President Regulatory Affairs, England. Vice President, Regulatory Affairs. Key Experience Regulatory relative required:.

Regulatory Affairs Associate - Devon -Up to £40,000 pa + benefits - Ref 1894. I am currently recruiting for a Regulatory Affairs Associate to work for a multi-national medical device organisation. This is a fantastic opportunity for a Regulatory Affairs Associate to work for a leader within their...

This position focuses on providing regulatory affairs support to both ongoing development programs as well as approved product lifecycle activities. Collaborate with Regulatory Project Management to create and align submission timelines. Assist with activities related to regulatory compliance and...

Senior Manager in Global Regulatory Affairs. Serve as the primary regulatory interface across internal functions and regulatory authorities. Significant experience in the pharmaceutical industry, including 5+ years in Regulatory Affairs.

In this role, you will ensure regulatory interactions are managed in a way that supports positive and transparent regulatory relationships with the FCA, TPR and FOS (the “regulators”); You will also ensure that those meeting the regulators are appropriately briefed, and full and accurate regulat

Proven experience in CMC regulatory affairs within the pharmaceutical or biotechnology industry. Ensure compliance with current regulatory guidelines and standards. Continuously improve CMC regulatory processes and systems to enhance efficiency and effectiveness.

Provide centralized support across Regulatory Affairs Advisory teams on their execution of assessing, interpreting, and advising on compliance obligations and readiness efforts throughout the regulatory life-cycle, including in external engagements. The Regulatory Affairs team helps the company i...

Regulatory and/or non-Regulatory systems that are critical for Regulatory submission and maintenance activities. Regulatory Affairs Manager - Global Clinical Trials. As the only Regulatory Affairs professional based in the UK, you must be confident with global clinical trial regulations and have ...