- Organon & Co. (Jersey City, NJ)
- … Director ) is responsible for developing and implementing Regulatory Chemistry , Manufacturing & Controls (CMC) strategies for assigned small molecule and/or ... lead the preparation and submission of CMC dossiers for programs in clinical development, marketing applications and post-approval life cycle maintenance phases. The… more
- Merck (Rahway, NJ)
- …for building and executing CMC development plans. Under the guidance of the CIPM Director & Portfolio Lead, the core responsibility of this individual will be to ... lead project management efforts to support Chemistry Manufacturing & Controls (CMC) product development from First in Human to Transfer to Supply, driving line of… more
- Hunterdon Health Care System (Flemington, NJ)
- …hospital support staff. Reporting Relationships Reports to (position): Director Laboratory Services Supervises (position(s): Medical Laboratory Scientists, Medical ... Qualifications Minimum Education: Required: Bachelor's Degree in chemical, biological, clinical laboratory science or medical technology from an accredited… more
- Atlantic Health System (Morristown, NJ)
- The Technical Director supports the Clinical disciplines of the laboratory such as Chemistry , Hematology, Microbiology, Specialty Testing, and Blood Bank to ... equipment vendors. The scope of responsibility for the Technical Director spans the entire clinical laboratory value...Clinical Pathology, or equivalent + Fellowship in a Clinical area of expertise Microbiology, Chemistry , … more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- Director , Formulation Development is an experienced leader in the development of pharmaceutical products in a virtual environment with extensive technical, strategic ... to work effectively with CDMOs. The position reports to Executive Director , CMC & Product Development. **Job Description** **Pharmaceutical Development:** + You… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... studies. + Collaborate cross-functionally with analytical team members, process chemistry , formulation development, regulatory affairs, quality assurance, and other… more
- Bristol Myers Squibb (Summit, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Senior Director , Cell Therapy Global Product Quality Lead ( Sr. Dir. CT- ... , control strategies, comparability, specifications, and stability . The Sr. Director m onitors commercial operations through periodic reviews of process and… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …self. Become a **maker of possible** with us. The Regulatory Affairs (RA) Director is responsible for the management and setting the direction for the Medication ... platform within the Medication Delivery Solution Business Unit. The RA Director is responsible for developing and implementing regulatory strategies and submissions… more
- Merck (Rahway, NJ)
- …through information science. We are seeking a passionate, experienced Associate Director to connect scientists and stakeholders with focused scientific literature ... knowledge services that empower research teams across the organization. As Associate Director , you will collaborate closely with cross-functional teams to design and… more
- Taiho Oncology (Princeton, NJ)
- …and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources ... At Taiho Oncology, we are leaders in cutting-edge science and technology, from chemistry to pharmacokinetics. This expertise and our unique vision allow us to… more