- Bristol Myers Squibb (Summit, NJ)
- …careers.bms.com/working-with-us . **Position Summary** Bristol Myers Squibb is seeking an Associate Director , Principal Product Leader within the Cell Therapy ... The Principal PQL will support the Global Product Quality Lead (PQL) by providing supportive quality oversight of the...+ May act as author or Quality reviewer of CMC sections of regulatory submissions and response to global… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …on real-world evidence, and creating hope for all facing illness. The Associate Director , Business Development will seek out potential business opportunities ... efficiently communicating with excellent facilitation. The incumbent will also lead initial partnership, licensing and/or acquisition negotiations with sufficient… more
- Merck (Rahway, NJ)
- …sight to process validation and commercial launch. This role reports into the Associate Vice President, Sterile Products Development. This role is located in Rahway, ... of sight to commercial production + Oversee and review CMC authoring activities for DP manufacturing + Ensure successful...process analysis and control throughout the lifecycle + Attract, lead , and develop a world-class team of scientists and… more
- AbbVie (Madison, NJ)
- …with multiple driver indications within a Therapeutic Area and support the Manager, Global Regulatory Lead (GRL), Associate Director , or Director , in the ... timely response to Health Authorities during application review. . Support CMC sections of major, complex regulatory submissions, including Investigation New Drugs… more