- Bristol Myers Squibb (Summit, NJ)
- …here at BMS with our Cell Therapy team. The **Manufacturing Associate , Liso-cel CAR-T, Manufacturing Operations** manufactures human blood derived components per ... the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed… more
- Bristol Myers Squibb (Summit, NJ)
- …place than here at BMS with our Cell Therapy team. Our Manufacturing Associate , Cell Therapy team manufactures human blood derived components per Batch Record and ... the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed… more
- dsm-firmenich (Belvidere, NJ)
- ** Associate Operator - Production** **Location: Belvidere, NJ (US)** **Onsite** **12 - Hour Rotating Shifts** As an ** Associate Operator** , you will be ... Current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs), safety/ regulatory requirements, and Site goals. This position is overtime… more
- J&J Family of Companies (Raritan, NJ)
- …Innovative Medicine is informed and inspired by patients, whose insights fuel our science -based advancements. Visionaries like you work on teams that save lives by ... at https://www.jnj.com/innovative-medicine We are searching for the best talent for the Associate Director, Global Medical Affairs Strategy & Execution to be in… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …managed, governed, and secured, following industry best practices and regulatory requirements. + Model Otsuka's core competencies (Accountability for Results, ... Research, Analytics, Otsuka Information Technology (OIT), Sales Operations, and Medical/ Regulatory /Legal integrated business partners. **Minimum Qualifications:** + Minimum bachelor's… more
- Bristol Myers Squibb (Summit, NJ)
- …continued investment in our Cell Therapy capabilities, the growth potential of this science , your career, and the ability to help patients are incredible. We are ... strategies, process risk assessments, etc), inspection readiness, and technical regulatory submissions. The Sr. Principal Engineer will support commercial product… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …Analytics, Otsuka Information Technology (OIT), Sales Operations, and Medical/ Regulatory /Legal integrated business partners. **Minimum Qualification:** + Bachelor's ... degree in data sciences, computer science and 4-6 years of relevant experience **Preferred Knowledge,...in the usage of machine learning/AI tools in life science area(s) and handling life science datasets… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …professional to join our organization as the Assoc. Director of Manufacturing Science and Technology (MSAT) for Upstream processes. This critical role will lead ... and/or review technical reports, protocols, risk assessments, and relevant sections of regulatory submissions (IND, BLA, MAA, etc.) related to upstream processing. +… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, WW Medical Cell Therapy Autoimmune, LCM/Pan-Indication, will report ... an understanding of pharmaceutical drug development including clinical development, regulatory , life cycle management of pharmaceutical products, and knowledge of… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Associate Director of Government Contracts will become a subject matter expert ... impact government gross-to-nets. + Interpret changing CMS guidance and new regulatory proposals as they are released. Quantify potential impact, adjust projection… more