An innovative and fast-growing life sciences consultancy is seeking a Senior Manager of Regulatory Affairs – CMC to support a diverse portfolio of biologic development programs. This fully remote opportunity is ideal for someone experienced in biologics CMC who thrives in a high-paced, client-facing...
CMC Manager - Antibody Drug Conjugates - Cambridge UK - Hybrid. You will be directly responsible for driving ADC programs through the IND/CMC process and into the clinic to treat individuals with cancer. ...
Walker Cole International is currently supporting hiring for a CMC Manager. Key Responsibilities of the CMC Manager: * Leading drug substance process development, validation, and regulatory submission. Key requirements for the CMC Manager position include: * Extensive experience in mammali...
The Regulatory Chemistry Manufacturing Controls (CMC) Manager will 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 with interactions with H...
Walker Cole International is currently supporting hiring for a CMC Manager. Key Responsibilities of the CMC Manager: * Leading drug substance process development, validation, and regulatory submission. Key requirements for the CMC Manager position include: * Extensive experience in mammali...
Senior Manager/ Associate Director / Director, CMC Business Development. Pharmaron is in search of an experienced Senior Manager/ Associate Director / Director in CMC Business Development, who is adept at navigating API development from early to clinical development and manufacturing. Strategize and...
As the CMC Regulatory Manager you will play a vital role in our companys worldwide postapproval regulatory activities specifically focused on Chemistry Manufacturing and Controls (CMC) for biological products. Develop submission strategies and plans for postapproval CMC activities such as variations...
CMC Manager - Antibody Drug Conjugates - Cambridge UK - Hybrid. You will be directly responsible for driving ADC programs through the IND/CMC process and into the clinic to treat individuals with cancer. ...
As the CMC Regulatory Manager, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products. Develop submission strategies and plans for post-approval CMC activities such as var...
We are seeking a highly skilled and proactive CMC Project Manager to oversee the CMC activities supporting our gene therapy programs. This pivotal role will involve coordinating crossfunctional teams to ensure the seamless of CMC strategies and delivery of highquality gene therapy products in compl...
As the CMC Regulatory Manager you will play a vital role in our companys worldwide postapproval regulatory activities specifically focused on Chemistry Manufacturing and Controls (CMC) for biological products. Develop submission strategies and plans for postapproval CMC activities such as variations...
They are seeking a Regulatory Affairs Manager (CMC) to join our Regulatory Affairs Team based in Cambridge on a 12 month contract. Co-ordinate the preparation of high quality CMC documents to support regulatory submissions in International regions, (Asia, Latin America, Middle East, Eastern Europe a...
They are seeking an experienced Project Manager to take full ownership of the implementation and lead the end-to-end process, working closely with multiple stakeholders across the business to ensure successful delivery. You will be an experience Project / Programme Manager who has experience of lead...
We are seeking a highly skilled and proactive CMC Project Manager to oversee the CMC activities supporting our gene therapy programs. This pivotal role will involve coordinating crossfunctional teams to ensure the seamless of CMC strategies and delivery of highquality gene therapy products in compl...
Senior Manager, Regulatory Affairs CMC - OxfordImmunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseas...
The Project Manager, CMC Regulatory Affairs will be responsible for the CMC regulatory activities in the investigational, late phase development and/or early commercial lifecycle management of GSK products. Responsible for CMC strategy development, with managerial support, for CMC submission documen...
At Orchard, the Regulatory Team provide Regulatory and Chemistry, Manufacturing and Control (CMC) - related expertise for development and commercial stage products, including developing strategies, and partnerships with key stakeholders to execute on the strategies in alignment with business priorit...
Global CMC RA organization serves as CMC RA Affiliate for assigned products and territories who through partnership with Global teams and full integration in RA Affiliate, design and execute CMC RA strategies that align PDM's (Pharmaceutical, Development, Manufacturing) CMC objectives with Affiliate...
Senior Manager, Regulatory Affairs, CMC-2407021125W. Senior Manager, Regulatory Affairs, CMC. The Senior Manager Regulatory Affairs (RA) leads a team responsible for the development of CMC/technical regulatory strategies across the EMEA region providing regulatory input and technical guidance on reg...
Our client are a PE backed company within the media sector, they are now seeking a commercially focussed qualified accountant to join them as FP&A Manager. ...