THE LARGEST COLLECTION OF MANAGERIAL JOBS ON EARTH
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... for the development of the CMC regulatory strategy for submissions. These submissions ... IND/CTA, NDA, CTD and MAA regulatory filings. Collaborate with other relevant ... functions to prepare and..
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 ..
... results. Functional Area Description The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages of ... of the organization develop global regulatory CMC strategies and partners..
... on internal/external system audits and regulatory agency inspections Responsible for business ... documentation system in compliance with regulatory requirements, company requirements and procedures; ... research, analytical, quality, engineering, manufacturing,..
... and transformative business results. The Director of Analytical CMC strategy is accountable for defining ... and executing the commercial analytical CMC strategy for BMS small and ... products. In..
... The primary focus of the Associate Director/Director, External Manufacturing, Cell Therapy role ... of objectives and priorities with CMC Strategy Team, representing the VPT ... but not limited to..
Job Information Bristol Myers Squibb Associate Director, Parenteral ExM MS&T in New ... business results. Job Function The Associate Director MS&T External Manufacturing Parenteral Drug ... Health Authorities in support..
... development strategy and all process-related CMC deliverables across multiple sites including ... implementation, platform process lifecycle strategy, regulatory submissions, and handoff to manufacturing ... with appropriate scale, GMP and..
... while maintaining existing products/processes. The Associate Director, MSAT Cell Therapy Engineering and ... This position reports to the Director, MSAT. DUTIES AND RESPONSIBILITIES: Lead ... Establish Frontline Support and..
... results. Functional Area Description The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages of ... of the organization develop global regulatory CMC strategies and collaborate..
... manage, and execute a complete CMC strategy for BMS biologics commercial ... develop and deliver on the CMC strategy while ensuring that the ... customer service targets, successfully achieving..
... Product Quality Lead (Principal PQL), Associate Director of Global Product Quality. The ... Development, Manufacturing Sciences and Technologies, Regulatory Affairs, and other Cell Therapy ... Therapy Development Organizations to..
... in technology transfers, process validation, CMC life cycle management, technical oversight ... therapy manufacturing network. As the Director of Vector/Gene Delivery MSAT you ... External Manufacturing, Supply Chain and..
... business results. Job Description: The Associate Director of GPS Business Development and ... the Chemistry, Manufacturing & Controls (CMC) and product supply aspects including ... functions, SME’s and governance..
... transformative business results. Summary The CMC Regulatory Associate Director is responsible for content development, ... of the Quality Module for regulatory submissions to support biotechnology products ... submissions. In..
... make a difference. Position: Executive Director, Regulatory Affairs Team Leader Supervisor: Vice ... Team Leader Supervisor: Vice President, Regulatory Affairs Department: Global Regulatory Affairs Prerequisites Bachelors in scientific .....
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 ..
