Regulatory affairs jobs in BeckenhamCreate job alerts

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...

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. The Director will be responsible for initiating and maintaining CMC regulatory strategic plans across various assets, identifying team synergies or conflicts early, and proposing effective solutions. ...

Senior Manager in Global Regulatory Affairs. Serve as the primary regulatory interface across internal functions and regulatory authorities. Senior Manager, Global Regulatory Affairs.

Extensive regulatory affairs experience in the UK, EU, and EMEA regions. An innovative biotech company focused on individualized genetic medicines is seeking an SVP/VP of Regulatory to lead its global regulatory strategy. Strong relationships with key regulatory agencies (UK, EU, and preferably F...

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. Cure Talent is delighted to be working with an innovative MedTech company r...

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 ...

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...

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...

The Senior Director, Regulatory Affairs is integral to designing and advancing the company’s effort to discover, develop and commercialize small molecule therapeutics for rare endocrine disorders and endocrine-related tumors. This role will report to the Vice President of Regulatory Affairs, Euro...

Regulatory Affairs Manager – Clinical Trials. Are you confident navigating complex global clinical trial regulations? Do you bring experience guiding research teams through the challenges of compliance in an evolving regulatory landscape and leading clinical trial submissions for CTIMPs and/or me...

Practical experience managing regulatory data in a controlled Regulatory Information Management to defined quality standards. The Regional RIM Support Specialist will support one or more Client’s Local Operating Companies (LOCs) for regulatory business process execution in the Regulatory Informat...

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.

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. Work with teams across clinical, pharmacovigilance, and brand management to align regulatory strategies with...

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...

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...

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

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...

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...

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. Manage regulato...

This is a unique opportunity for a deeply knowledgeable and well-connected regulatory professional to help shape Bloomberg's engagement on key policy and regulatory developments - in the UK, across Europe, and globally. Deep knowledge of the UK and EU regulatory landscape. ESG and sustainable fin...

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...

Senior Director, Regulatory Affairs, EMEA Defense Lead. Regulatory Affairs helps the company innovate responsibly and comply with laws around the world. As Senior Director, Regulatory Affairs, EMEA Defense Lead, you’ll join an EMEA-based team addressing the highest and emerging risks pertaining t...

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.

Set priorities and work with Regulatory Affairs consultants, Quality, Manufacturing, MSAT, Pharmacovigilance, and Medical Affairs teams to ensure smooth submissions and approvals. As the Director of Regulatory Affairs, you will lead and execute regulatory strategies for biologic products, ensurin...

This is a unique opportunity for a deeply knowledgeable and well-connected regulatory professional to help shape Bloomberg’s engagement on key policy and regulatory developments — in the UK, across Europe, and globally. Bloomberg through strategic policy briefings and updates, enabling informed

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

Director of Regulatory Affairs CMC, London. Proven experience in CMC regulatory affairs within the pharmaceutical or biotechnology industry. Continuously improve CMC regulatory processes and systems to enhance efficiency and effectiveness.

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...

Senior Manager, Global Regulatory Affairs. Senior Manager, Global Regulatory Affairs, London. Global Regulatory Affairs (GRA) team.

Regulatory and/or non-Regulatory systems that are critical for Regulatory submission and maintenance activities. 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...

Participate in other Regulatory Affairs projects and supporting other team members. At least 1-2 years’ experience in Regulatory Affairs (labelling) is preferable. Maintain records of tasks and registered product information in the internal regulatory databases.

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...

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

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...

With a growing regulatory team, an exciting opportunity has emerged for a Manager, Regulatory Affairs to contribute to the development of cutting-edge cell and gene therapy products. This role involves working within a global regulatory affairs team, overseeing the planning, preparation, review, ...

Proven experience in CMC regulatory affairs within the pharmaceutical or biotechnology industry. Director, CMC Regulatory Processes and Systems. The Director will be responsible for initiating and maintaining CMC regulatory strategic plans across various assets, identifying team synergies or conf...

This position focuses on providing regulatory affairs support to both ongoing development programs as well as approved product lifecycle activities. With oversight by EU lead, develop and coordinate content for EU regulatory submissions, for example Orphan Drug designation, Module 1 of EU MAA. Co...

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

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...