Post-Approval Regulatory Expert

Lifelancer is seeking a highly qualified Principal Regulatory Affairs Consultant to join our team. As an Associate Director level professional, you will be responsible for providing expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule development.This role offers a unique opportunity to showcase your technical skills, specialist...

About the RoleLifelancer is seeking an experienced Regulatory Affairs Consultant to join our team as a Principal Advisor. This is an exciting opportunity to lead and implement post-approval Chemistry, Manufacturing, and Controls (CMC) strategies for small molecule clients.Key ResponsibilitiesProject Leadership: Serve as a project leader, ensuring successful...

We are seeking an experienced regulatory professional to join our dynamic team as a Compliance Manager. This is a client dedicated project, and the role can be office or home based in various European locations.The successful candidate will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry,...

Parexel, a leading Clinical Research Organization (CRO), seeks an expert in Chemistry, Manufacturing, and Controls (CMC) for small molecule regulatory affairs. As a Principal Regulatory Affairs Consultant, you will lead post-approval CMC activities, providing strong project management skills and regulatory knowledge.This role offers flexibility with home or...

Parexel International is currently seeking a highly skilled Compliance Manager to join our team. As a key member of our regulatory department, you will play a crucial role in ensuring compliance with regulatory requirements for our clients.The ideal candidate will have a strong background in regulatory affairs, specifically in the area of Chemistry,...

Parexel is seeking a highly skilled Senior Regulatory Affairs Manager for biologics to join our team in the European region. This role can be performed from home or office locations.The ideal candidate will play a crucial role in worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological...

Candidates for the Pharmaceutical Industry Regulatory Expert role will lead the procedural and operational aspects of European regulatory filings within the Centralised Procedure. This includes planning and tracking activities, communicating regulatory information, and providing logistical support for meetings.What You'll Do:Develop and implement strategies...

About the Role:The Global Regulatory CMC Director will be responsible for developing and implementing global regulatory strategies for cell therapy products, ensuring compliance with current regulations and guidelines.Key Responsibilities:Represent regulatory CMC on and/or lead matrix teams for cell therapy pipeline products and/or commercial products...

Job Description PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid. To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid.To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid.To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid.To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid.To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid. To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

About NorgineWe are a leading healthcare organisation dedicated to bringing innovative medical solutions to patients worldwide. Our company is built on a strong foundation of values, including our commitment to patient well-being, employee development, and community engagement.As a Medical Regulatory Affairs Specialist at Norgine, you will play a critical...

Proclinical are recruiting for a Senior Regulatory Consultant - Oncology to join a pharmaceutical organisation. This role is on a contract basis with the ability to work remotely from anywhere in the UK. **Responsibilities**: - Guide the development of regional regulatory documents and meetings rendering to GRT methods. - Cooperation share regulatory...

Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (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...

When our values align, there's no limit to what we can achieve.   Parexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong...

Your new companyGlobal Biotechnology in the UK is looking for a Regulatory Affairs Senior Manager to develop and implement regulatory strategies for EU markets for their Oncology portfolio in development. This position will sit within the global regulatory team and will require someone to have both development and post-marketing experience.Your new roleAs a...

Your new company Global Biotechnology in the UK is looking for a Regulatory Affairs Senior Manager to develop and implement regulatory strategies for EU markets for their Oncology portfolio in development. This position will sit within the global regulatory team and will require someone to have both development and post-marketing experience. As a member...