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Legal Director, Regulatory Affairs & Compliance - 10+pqe - London. Director of Regulatory Affairs & Compliance,. FCA, consumer duty and other relevant financial services regulatory and legal frameworks.

Implement optimal regulatory strategies for each programme in agreement with the Head of Regulatory Affairs/Senior Lead Regulatory Affairs, Chief Clinical Officer (CCO) and key stakeholders. Implement optimal regulatory strategies for each programme in agreement with the Head of Regulatory Affair...

POSITION SUMMARY The Regulatory Affairs Specialist reports directly to the Director of Global Regulatory Affairs. WORK EXPERIENCE REQUIREMENTS Professional Experience – demonstrable experience in regulatory affairs is preferred. Bachelor’s Degree in Regulatory Affairs, Food Science, Chemistry, B

Develop and implement policies and procedures for regulatory affairs. Minimum 10+ year experience in regulatory affairs with experience in the food industry and an understanding of related issues. Head of Regulatory Affairs, EMEA.

Experience in CMC Regulatory Affairs within the pharmaceutical or biotechnology industry. Job title: Senior Regulatory Affairs Manager CMC. A growing pharmaceutical business in London are seeking a Senior Regulatory Affairs Manager CMC to join their team.

Minimum 10+ year experience in regulatory affairs with experience in the food industry and an understanding of related issues. Head of Regulatory Affairs, EMEA. Develop and implement policies and procedures for regulatory affairs.

Reporting to the Regulatory Affairs Manager, this strategic position involves preparing and submitting regulatory applications in key markets in the EU, acting as Project lead in support of the new product development programme and renewal of existing product authorisations. The ideal candidate w...

Reporting to the Regulatory Affairs Manager, this strategic position involves preparing and submitting regulatory applications in key markets in the EU, acting as Project lead in support of the new product development programme and renewal of existing product authorisations. The ideal candidate w...

Implement optimal regulatory strategies for each programme in agreement with the Head of Regulatory Affairs/Senior Lead Regulatory Affairs, Chief Clinical Officer (CCO) and key stakeholders. With the Head of Regulatory Affairs and/or Senior Lead Regulatory Affairs, develop an agreed CMC/ regulato...

Implement optimal regulatory strategies for each programme in agreement with the Head of Regulatory Affairs/Senior Lead Regulatory Affairs, Chief Clinical Officer (CCO) and key stakeholders. Implement optimal regulatory strategies for each programme in agreement with the Head of Regulatory Affair...

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. Ideal background: 3+ years in energy policy and regulatory affairs in the German market. If y...

Create and deliver high-quality billable regulatory related documentation for clients, contributing to the technical authorship and review of development regulatory documents including Regulatory Strategy Plans, Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advic...

Planet Pharma are currently working on an exciting opportunity with a global biopharmaceutical company that’s looking to expand its Regulatory Affairs team. If you have 3–5+ years’ experience in regulatory affairs, particularly in emerging markets, and enjoy cross-functional collaboration with

If you are a seasoned Regulatory professional within the Medical Device space, this role might be for you! We’re looking for a Regulatory Consultant who can support a diverse portfolio of clients with particular expertise in medical device software (SaMD) and AI/ML technologies. Develop and imple...

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Planet Pharma are partnered with a leading pharmaceutical company and we are actively seeking an exper...

Senior Vice President / Vice President of Regulatory Affairs. This executive role will lead global regulatory strategy, with a particular focus on the UK and EU, supporting the development of advanced genetic therapies using ASO technologies. Lead regulatory strategy and submissions across the UK...

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Planet Pharma are partnered with a leading pharmaceutical company and we are actively seeking an exper...

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

If you are a seasoned Regulatory professional within the Medical Device space, this role might be for you! We’re looking for a Regulatory Consultant who can support a diverse portfolio of clients with particular expertise in medical device software (SaMD) and AI/ML technologies. Develop and imple...

Senior Vice President / Vice President of Regulatory Affairs. Lead regulatory strategy and submissions across the UK, EU, and potentially the US. Liaise with MHRA, EMA, and other authorities to ensure regulatory alignment.

Minimum 10+ year experience in regulatory affairs with experience in the food industry and an understanding of related issues. Head of Regulatory Affairs, EMEA. Develop and implement policies and procedures for regulatory affairs.

The Regulatory Affairs Specialist reports directly to the Director of Global Regulatory Affairs. Professional Experience – demonstrable experience in regulatory affairs is preferred. Bachelor’s Degree in Regulatory Affairs, Food Science, Chemistry, Business Administration or related field is req

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Key Responsibilities: - Shape and implement regional regulatory strategy by advising the Global Regula...

A fast-growing and forward-thinking life sciences consultancy is seeking an Associate Director of Regulatory Affairs – CMC to lead regulatory strategy and execution across a dynamic portfolio of biologic and advanced therapy programs. CMC Regulatory Affairs, with strong biologics expertise (e. As...

POSITION SUMMARY The Regulatory Affairs Specialist reports directly to the Director of Global Regulatory Affairs. Bachelor’s Degree in Regulatory Affairs, Food Science, Chemistry, Business Administration or related field is required - Knowledge of the Food & Beverage or Consumer Packaged Goods (C...

Planet Pharma are currently working on an exciting opportunity with a global biopharmaceutical company that’s looking to expand its Regulatory Affairs team. If you have 3–5+ years’ experience in regulatory affairs, particularly in emerging markets, and enjoy cross-functional collaboration with

Key Responsibilities - Develop and implement regulatory strategies for assigned programs at regional or global levels - Serve as the primary regulatory interface across internal functions and regulatory authorities - Provide strategic regulatory input into target product profiles and integrated a...

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Planet Pharma are partnered with a leading pharmaceutical company and we are actively seeking an exper...

Key Responsibilities - Develop and implement regulatory strategies for assigned programs at regional or global levels - Serve as the primary regulatory interface across internal functions and regulatory authorities - Provide strategic regulatory input into target product profiles and integrated a...

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Senior Regulatory Affairs Manager - Emerging Markets. We are currently looking for a Snr Regulatory Af...

Regulatory Affairs Manager - Pharmaceuticals As the Regulatory Affairs Manager for the UK and Ireland, you will provide expert regulatory guidance to our UK organization and manage all regulatory activities across the UK and Ireland. Liaise with regulatory authorities and maintain up-to-date know...

Minimum of 10 years’ experience in regulatory affairs or chemical compliance in FMCG/CPG, personal care, beauty, or food industries. Associate Director – Global Regulatory Affairs (EPR & Chemical Compliance). Associate Director of Global Regulatory Affairs.

Job Description Associate Director – Global Regulatory Affairs (EPR & Chemical Compliance) Are you an experienced regulatory leader with deep expertise in global EPR and chemical compliance? We're looking for an Associate Director of Global Regulatory Affairs to take the lead on international che...

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

Position Summary We are seeking an experienced freelance CMC Regulatory Affairs Consultant to support the development, submission, and lifecycle management of regulatory CMC documentation for biologics, pharmaceuticals and/or advanced therapies. Serve as a liaison between Regulatory Affairs, Manu...

The Regulatory Affairs Specialist reports directly to the Director of Global Regulatory Affairs. Professional Experience – demonstrable experience in regulatory affairs is preferred. Bachelor’s Degree in Regulatory Affairs, Food Science, Chemistry, Business Administration or related field is req

Role: Senior Regulatory Affairs Manager - Emerging Markets Location: Remote, UK Company: Global Pharmaceutical We are currently looking for a Snr Regulatory Affairs Manager with experience in Emerging Markets including Middle East Africa (MEA), Turkey, CIS & Russia (TCR) and Central Eastern Europ...

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Planet Pharma are partnered with a leading pharmaceutical company and we are actively seeking an exper...

POSITION SUMMARY The Regulatory Affairs Specialist reports directly to the Director of Global Regulatory Affairs. Regulatory Affairs Specialist COMPANY DESCRIPTION ASR Group is the world’s largest refiner and marketer of cane sugar, with an annual production capacity of more than 6 million tons o...

If you are a seasoned Regulatory professional within the Medical Device space, this role might be for you! We’re looking for a Regulatory Consultant who can support a diverse portfolio of clients with particular expertise in medical device software (SaMD) and AI/ML technologies. Provide regulator...

Overview Reporting to the Regulatory Affairs Manager, this strategic position involves preparing and submitting regulatory applications in key markets in the EU, acting as Project lead in support of the new product development programme and renewal of existing product authorisations. The ideal ca...

Create and deliver high-quality billable regulatory related documentation for clients, contributing to the technical authorship and review of development regulatory documents including Regulatory Strategy Plans, Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advic...

Job Title: Associate Director - Regulatory Research & Intelligence (Maternity Cover).

As the Regulatory Affairs Manager for the UK and Ireland, you will provide expert regulatory guidance to our UK organization and manage all regulatory activities across the UK and Ireland. With several exciting drug launches planned over the next 24 months, we are looking for a dedicated and expe...

Implement optimal regulatory strategies for each programme in agreement with the Head of Regulatory Affairs/Senior Lead Regulatory Affairs, Chief Clinical Officer (CCO) and key stakeholders Compile and submit regulatory submissions, ensuring that they are delivered to agreed time, cost and qualit...

Minimum of 5 years of experience in the pharmaceutical or biotechnology industry, with a focus on Regulatory Affairs—preferably within International or Emerging Markets. Planet Pharma are currently working on an exciting opportunity with a global biopharmaceutical company that’s looking to expan

Monitor and interpret updates from FDA and EMA, including new proposals, approvals, and regulatory shifts Identify and synthesise relevant clinical trial, labelling, and approval precedents to inform strategic planning Collaborate closely with Global and US Regulatory Leads, as well as cross-func...

Senior Vice President / Vice President of Regulatory Affairs. Lead regulatory strategy and submissions across the UK, EU, and potentially the US. Liaise with MHRA, EMA, and other authorities to ensure regulatory alignment.