Regulatory Affairs Director, CMC Lead

Otsuka Pharmaceutical Europe seeks a highly skilled Director CMC Regulatory Affairs to provide expertise on CMC regulatory matters for investigational and marketed products.The successful candidate will establish CMC regulatory strategies, ensuring Otsuka's products comply with global regulatory requirements. They will anticipate, develop, and recommend...

Regulatory Affairs ConsultantParexel Consulting is seeking a seasoned CMC Regulatory Affairs Professional to collaborate with our team. As a Regulatory Affairs Consultant, you will utilize your expertise in CMC, excellent communication skills, and strong writing experience to contribute to our clients' success in the pharmaceutical industry.Key...

Overview of the RoleThis exciting opportunity is for a highly skilled and experienced Director of Regulatory Affairs, CMC to join our team at GlaxoSmithKline. As a key strategic partner, you will play a crucial role in representing Global Regulatory activities and driving strategic direction on global project and key business initiatives.Job DescriptionWe...

Job DescriptionParexel Consulting seeks a seasoned CMC Regulatory Affairs Professional as a Regulatory Affairs Consultant. This role offers the opportunity to utilize expertise in CMC, exceptional communication skills, and strong writing experience, contributing to clients' success in the pharmaceutical industry.Key Responsibilities:Assisting in technical...

OverviewWe are seeking a highly skilled Regulatory Affairs Manager to join our team at the Regulatory Affairs Professionals Society. As a key member of our organization, you will be responsible for overseeing regulatory strategy and ensuring compliance within our ingredient agent, brokerage, and solution manufacturing businesses.

About Us: GlaxoSmithKline (GSK) is a global biopharma company with a special purpose – to unite science, technology, and talent to get ahead of disease together.Job Summary: We are seeking an experienced Director of Policy and Regulatory Affairs to lead key strategic CMC regulatory activities for investigational and early commercial biological products.Key...

About the Role:As a CMC Director, you will be responsible for providing strategic direction and guidance on both global project and key strategic business initiatives within Global Regulatory Affairs. You will lead key, strategic CMC regulatory activities for investigational and early commercial biological products, and drive the CMC strategy to support...

About the Role: We are looking for an experienced professional to join our team as a Director of Policy and Regulatory Affairs. This role will be responsible for leading key strategic CMC regulatory activities for investigational and early commercial biological products.Key Responsibilities:Lead key, strategic CMC regulatory activities for investigational...

Company Overview: As a global biopharma company, GlaxoSmithKline (GSK) is dedicated to uniting science, technology, and talent to get ahead of disease together.Salary: $150,000 - $200,000 per yearJob Description: We are seeking an experienced Director of Policy and Regulatory Affairs to lead key strategic CMC regulatory activities for investigational and...

Job DescriptionParexel Consulting is a leading provider of CMC Regulatory Affairs Services. We are seeking a highly skilled and experienced professional to join our team as a Regulatory Affairs Specialist.In this role, you will have the opportunity to leverage your expertise in CMC, exceptional communication skills, and strong writing experience to...

Vertex Job Opening: Regulatory CMC ManagerJob Summary:The Regulatory Chemistry Manufacturing Controls (CMC) Manager will significantly contribute to the execution of global regulatory CMC strategies for investigational and marketed products at Vertex. This role will prepare and submit regulatory CMC documentation, interact with Health Authorities for CMC...

Parexel Consulting is seeking a highly skilled Regulatory Affairs Consultant to join our team.">About the Job:">We are looking for an experienced professional with expertise in Clinical Trial Management and strong communication skills to contribute to the success of our clients in the pharmaceutical industry. This position offers exposure to novel...

Job DescriptionAt GSK, we're on a mission to unite science, technology, and talent to get ahead of disease together. As a key member of our Global Regulatory Affairs team, you'll play a critical role in ensuring the timely preparation and submission of regulatory documents to support the development, registration, and lifecycle maintenance of our...

Job DescriptionAs a key strategic partner, you will represent Global Regulatory activities and provide strategic direction and guidance on global project and key strategic business initiatives. This role will lead key, strategic CMC regulatory activities for investigational and/or early commercial biological products.Key ResponsibilitiesLeads CMC regulatory...

Parexel Consulting is seeking a skilled Regulatory Affairs Consultant to join our team.">About the Role:">We are looking for an experienced professional with expertise in Clinical Trial Management and strong communication skills to contribute to the success of our clients in the pharmaceutical industry. This position offers exposure to novel technologies and...

Job Title: Regulatory CMC ManagerJob Summary:Vertex is seeking a highly skilled Regulatory CMC Manager to influence the execution of multi-product global regulatory CMC strategies for investigational and marketed products. This role contributes to the preparation and submission of regulatory CMC documentation and interactions with Health Authorities for CMC...

About the JobThe Regulatory Chemistry Manufacturing Controls (CMC) Manager will play a key role in Vertex's execution of multi-product global regulatory CMC strategies for investigational and marketed products.This role contributes to the preparation and submission of regulatory CMC documentation and interactions with Health Authorities for CMC topics....

Job DescriptionThe CMC Development Projects Regulatory Project Manager plays a pivotal role in the global regulatory activities for assigned projects, ensuring seamless execution and compliance with regulatory standards.Key Responsibilities:Develop and implement CMC regulatory strategies for global submissions, from early phase clinical trials to marketing...

Job TitleRegulatory Affairs Lead (#J-18808-Ljbffr)About the CompanyAdvanced Accelerator Applications (Italy) - S...Job DescriptionThe Senior Regulatory Affairs Manager is a key member of our team, responsible for all aspects of submission, approval and life-cycle management of assigned Marketing Authorisations (MAs). They provide effective regulatory support...

Job Description:We are seeking a highly skilled Regulatory Affairs Leader to join our team at GlaxoSmithKline. In this role, you will be responsible for leading key strategic CMC regulatory activities for investigational and early commercial biological products.The successful candidate will have significant direct CMC regulatory experience, including...