THE LARGEST COLLECTION OF JOBS ON EARTH
Supports PDF, DOC, DOCX, TXT, XLS, WPD, HTM, HTML files up to 5 MB
... Description The GRS-CMC organization provides regulatory expertise related to CMC activities ... of the organization develop global regulatory CMC strategies and partners with ... priorities. The team also perform..
... a strong foundation in molecular biology and demonstrated experience working in ... the stewardship of late-phase molecular biology methods in the Quality organization. ... maintenance programs to support molecular..
Join a Legacy of Innovation 110 Years and Counting!nDaiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet ..
Job Information Bristol Myers Squibb Sr Manager Quality Compliance Cell Therapy in Summit New Jersey At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through ..
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and ..
Senior IP Counsel The candidate will seamless cooperation and collaboration with the Global Patent Attorney (and through them the global product development team working on a project) for each product, ensuring ..
Job DescriptionnnNew hires in office-based roles in the US & Puerto Rico will be required, subject to applicable law, to demonstrate that they have been fully vaccinated for COVID-19 or qualify ..
... Description The GRS-CMC organization provides regulatory expertise related to CMC activities ... of the organization develop global regulatory CMC strategies and partners with ... Summary / Objective The CMC..
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas ..
Research Scientist Come discover what our 25,000 employees already know: work here matters everywhere. We're a growing and evolving biopharmaceutical industry leader, which means you'll have endless opportunities to work with ..
... the development of the CMC regulatory strategy for submissions. These submissions ... IND/CTA/BLA, NDA, CTD and MAA regulatory filings. Support project teams (e.g. ... and line extensions. Interact with..
... / Objective To author complex regulatory documents ensuring the coordination and ... of the scientific, medical and regulatory input from development team members. ... that are compliant with established..