Regulatory CMC Project Lead

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...

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...

We are seeking a skilled Regulatory CMC Project Manager to join our team at RBW Consulting.The successful candidate will be responsible for overseeing regulatory activities for a small molecule oncology product globally.This role involves working independently and with an outsourcing team on tasks such as change controls, out of specification assessments,...

Opportunity OverviewWe are seeking a highly skilled Regulatory Affairs Director to lead our Chemistry, Manufacturing and Controls (CMC) team. This role will provide strategic direction and guidance on global project and key business initiatives.The successful candidate will have significant experience in leading CMC regulatory activities for investigational...

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 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...

Job DescriptionThis Senior CMC Regulatory Document Specialist role is responsible for preparing and submitting high-quality CMC regulatory documents to support registration activities for both small molecule and biopharmaceutical therapeutic assets.ResponsibilitiesPrepare, review, and finalize regulatory submission documents for late-stage clinical...

CPL Life Sciences is collaborating with a global pharmaceutical company focused on the discovery, development, and commercialization of innovative medicines.As a Senior Regulatory CMC Expert, you will be responsible for the development of CMC Strategy for a range of projects in the development phase, including the preparation of CMC submissions for...

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...

CMC Markets is a leading online financial trading business that has been operating since 1989. With offices and branches in 13 countries, we offer a unique opportunity for a talented lawyer to join our global team.As a Legal Counsel at CMC Markets, you will be part of a full-service legal team that provides advice on capital markets, trading-related, and...

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...

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...

Job TitleSenior CMC Regulatory Document SpecialistAbout the RoleThis pivotal position is instrumental in preparing and submitting high-quality CMC regulatory documents to support registration activities for both small molecule and biopharmaceutical therapeutic assets.Key ResponsibilitiesPrepare, review, and finalize regulatory submission documents for...

About UsRBW Consulting is a dynamic and innovative consulting firm that specializes in regulatory affairs for the pharmaceutical industry.Job OverviewWe are seeking a Senior CMC Regulatory Document Specialist to join our team and contribute to the development of groundbreaking therapies by ensuring the highest quality in regulatory...

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...

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...

**Orchard Therapeutics: A Leader in Gene Therapy Development**We are seeking an experienced CMC Project Manager to lead our advanced therapies project team.About the Role:Collaborate with cross-functional teams, including research, clinical, commercial, regulatory, and tech ops to develop target product profiles and ensure timely delivery of 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 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...