- Bristol Myers Squibb (Princeton, NJ)
- …The Development DMPK team is responsible for characterizing the ADME properties, and drug -interaction potential of drug candidates. Working closely with drug ... the globe. PCO is looking for a Scientific Director, Drug Metabolism to lead biotransformation activities in Development DMPK...years of academic and / or industry experience OR PhD or equivalent advanced degree in the Life Sciences… more
- Merck (Rahway, NJ)
- …or related science with 10 years of industrial experience with pharmaceutical drug substance and/or product development. + Ph.D. in chemistry or related science ... with 7 years of industrial experience with pharmaceutical drug substance and/or product development. **Required Skills:** + Demonstrated ability in leading teams. +… more
- Merck (Rahway, NJ)
- …& Technology (DD&T) organization designs, develops, and commercializes novel biologic/ drug / vaccine - device enabled combination products to achieve safe and ... set direction for the device development strategy for multiple drug -device combination product development programs ranging from concept generation/selection,… more
- Merck (Rahway, NJ)
- …devices (components, sub-assemblies, and full devices) and combination products ( drug -delivery products). This position will be responsible for technical ... interrogation of the various drug delivery device technology platforms supporting our company's pipeline...material and functional properties and attributes. Many of the drug delivery device technology platforms are often assemblages of… more
- Merck (Rahway, NJ)
- **Job Description** **Join Our Team as a Biologics Drug Substance Commercialization Leader!** Are you ready to take your career to the next level? We are seeking a ... and commercialization projects. **Why You'll Love This Role:** As a Biologics Drug Substance commercialization Leader, you'll be at the forefront of scientific… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …**** The Associate Director, MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing processes for the company's ... biologics portfolio executed at CDMOs. This role is responsible for ensuring the robustness, scalability, and compliance of downstream operations through effective technology transfer, validation support, process monitoring, troubleshooting, and lifecycle… more
- Merck (Trenton, NJ)
- …in biological sciences, chemistry, or related discipline with 10+ years of relevant drug development, clinical, or regulatory experience. + MD or Ph.D./Pharm D with ... 7+ years of experience. **Required Experience and Skills** + Proven ability to operate independently with minimal direction and deliver results. + Strong strategic thinking, problem-solving, and continuous learning mindset. + Effective communicator-both… more
- Bristol Myers Squibb (Princeton, NJ)
- …a department within the Research organization that facilitates the transition of drug candidates from early to late-stage clinical development, their approval and ... dose-schedule and responsive patient populations, based on deep understanding of drug mechanism of action and disease segments. Late-stage translational development… more
- Bristol Myers Squibb (Princeton, NJ)
- …a department within the Research organization that facilitates the transition of drug candidates from early to late-stage clinical development, their approval and ... dose-schedule and responsive patient populations, based on deep understanding of drug mechanism of action and disease segments. Late-stage translational development… more
- Bristol Myers Squibb (Princeton, NJ)
- …DMPK Team provides ADME (absorption, distribution, metabolism, and excretion), DDI ( drug - drug interactions) and PK (pharmacokinetics) support for all pipeline ... The Dev DMPK team is responsible for characterizing the ADME properties, and drug -interaction potential of drug candidates. Working closely with drug … more