GLOBAL REGULATORY AFFAIRS CMC jobs in UNITED STATES, United Kingdom #4

do, then you’re our kind of person. Oncology Regulatory Science and Strategy We are recruiting Regulatory Affairs professionals... Affairs Director (RAD), Oncology Cell and Gene Therapy provides strategic regulatory leadership to influence the development...

Would you like to apply your Regulatory Affairs strategy expertise and passion to make an impact in a company... to patients as efficiently and optimally as possible. The Regulatory Affairs Director (RAD) provides strategic and operational...

their skills. The Associate Director, Regulatory Affairs will be responsible for developing and implementing global regulatory... ICH and regional requirements, and have an understanding of current global and regional trends in regulatory affairs...

global regulatory strategies encompassing clinical, non-clinical and CMC disciplines. Ensures timely preparation of organized... ICH and regional requirements, and have an understanding of current global and regional trends in regulatory affairs...

. Interest in building a career in Regulatory Affairs. Strong knowledge of eCTD elements and structure including CMC... development. Responsibilities include: Assist in the authoring, submission, and maintenance of global regulatory submissions...

our innovative manufacturing approach to cell and gene therapies. We are seeking a global Executive Director, Regulatory Affairs... strategic lead representing regulatory affairs expertise managing the strategy and operational aspects of all regulatory...

your day Teva Pharmaceuticals USA, Inc. is seeking multiple Managers, Regulatory Affairs (Parsippany, NJ) to evaluate change... and qualifications Requires a Bachelor's degree in Pharmacy Administration, Pharmaceutical Science, Regulatory Affairs, or a related...

The Associate Director, Regulatory Affairs at 4DMT, will be focusing on managing CMC, pre-clinical, and clinical..., contract research organizations, and partners. Provide regulatory advice to clinical operations, CMC and pharmacology...

experience in global CMC regulatory affairs and CMC technical areas of at least 20 years with a BA/BS, MA/MS, PhD or PharmD.... Lead global CMC regulatory strategies for projects in development and marketed products, including risk mitigation...

of groundbreaking scientists today and change the world tomorrow. External Description The Head of Regulatory Affairs is a leadership... position responsible for the strategic oversight of all regulatory affairs activities related to the development...

search of an accomplished and dynamic Senior Director of Regulatory Affairs to join our team. This pivotal role... interactions with agencies, ensuring accuracy, completeness, and timeliness. Provide guidance on Regulatory CMC strategy...

line to the Global VP of Regulatory Affairs and Quality Assurance (RAQA) for Intuitive. The role will assume leadership... purpose of the Director of Regulatory Affairs, Imaging Agent Drug Development is to lead cross functional teams in major...

to the Senior Director of Global Regulatory Affairs with the primary objective to execute and pull through regulatory...Associate Director/Director, Regulatory Affairs Submissions and Operations Position Summary: This role reports...

of US regulatory affairs? We're seeking a dynamic individual to join our team, where you will play a key role in ensuring the accuracy... and timeliness of regulatory submissions for medical devices and software-driven medical devices. As a Regulatory Affairs...

questions within defined timelines. Perform assessment of CMC changes, identifying global regulatory requirements...Responsibilities: Author and review high-quality, compliant CMC regulatory documents (e.g., Core Dossiers, INDs, CTAs...

within CMC will facilitate product development and global registration by developing and executing regulatory strategies... and effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle...

within CMC will facilitate product development and global registration by developing and executing regulatory strategies... and effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. Title...