Regulatory affairs jobs in GreenfordCreate job alerts

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...

Housing Regulation & Partnerships Manager.Permanent, Full - time, 36 hours per weekAbout us at Hounslow.We’d love you to join us at the London Borough of Hounslow! Our people are deeply committed to providing excellent services to our residents, doing all we can.

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.

Job Title - Housing Regulation & Improvement ManagerPermanent, Full- time, 36 hours per week.Salary £52,584 - £55,620 per annum.About us at HounslowWe’d love you to join us at the London Borough of Hounslow! Our people are deeply committed to providing excellent services to our residents,.

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.

Senior Scientific and Regulatory Affairs Associate – Contaminants & Packaging. As an associate of Scientific & Regulatory Affairs, you'll performs a variety of.

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...

Job Title - Housing Regulation & Improvement ManagerPermanent, Full- time, 36 hours per week.Salary £52,584 - £55,620 per annum.About us at HounslowWe’d love you to join us at the London Borough of Hounslow! Our people are deeply committed to providing excellent services to our residents,.

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

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

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...

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 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.

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...

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...

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...

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...

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...

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...

Your Expertise & Impact Lead development and execution of regulatory strategies for clinical-stage oncology products Lead EU CTR Submission strategies Guide products through critical regulatory milestones from early development to market approval Foster collaborative relationships with health aut...

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...

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...

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...

If you have 3–5+ years’ experience in regulatory affairs, particularly in emerging markets, and enjoy cross-functional collaboration with global stakeholders, this could be a fantastic next step. Minimum of 5 years of experience in the pharmaceutical or biotechnology industry, with a focus on Re

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...

We are searching for a Global Regulatory Affairs Manager who will be managing and implementing EU/US/ROW Regulatory strategies for a recently in licensed product. Minimum of 5 years Regulatory Affairs experience, with working knowledge in EU and/or International markets. This role will take the l...

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

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

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...

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 knowledge of regulatory requirements. Regulatory ...

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.

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...

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. Senior Regulatory Affairs Manager - Emerging Markets. We are currently looking for a Snr Regulatory Af...

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...

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...

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...

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

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...

Senior Vice President / Vice President of Regulatory Affairs. Represent the company in external regulatory forums and industry groups. Scale regulatory operations during rapid organizational growth.

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...

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...

If you have 3–5+ years’ experience in regulatory affairs, particularly in emerging markets, and enjoy cross-functional collaboration with global stakeholders, this could be a fantastic next step. Minimum of 5 years of experience in the pharmaceutical or biotechnology industry, with a focus on Re

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...

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. Contribute to internal regulatory intelligence and advise cros...