- Organon & Co. (Plymouth Meeting, PA)
- …to the Director in Regulatory Chemistry, Manufacturing and Controls, the Senior Scientist is responsible for implementing Regulatory Chemistry, ... products in accordance with global regulations, guidance's and defined regulatory strategies. The Senior Scientist is responsible for the preparation and… more
- Merck (North Wales, PA)
- …product withdrawal. + Support new technology development. + Demonstrate an understanding of regulatory affairs and applies this understanding to the benefit of ... **Job Description** Under general supervision of an Executive Director/ Senior Director, the Principal Scientist /Director is responsible for developing and… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... talented and dedicated colleagues while developing and expanding your career. The Senior Director ( Senior Principal Scientist ) has primary responsibility… more
- Merck (West Point, PA)
- …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) + ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
- Charles River Laboratories (Wayne, PA)
- …above. * Certification/Licensure: None. * Other: Demonstrated knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries ... you can feel passionate about. **Job Summary** Serve as the Principle Scientist responsible for the management and scientific oversite of assigned studies within… more
- Charles River Laboratories (Wayne, PA)
- …above. * Certification/Licensure: None * Other: Demonstrated knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries ... you can feel passionate about. **Job Summary** Serve as the Principal Scientist responsible for the development and execution of highly complex method development… more
- Charles River Laboratories (Wayne, PA)
- …above. * Certification / Licensure: None * Other: Knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries is ... career that you can feel passionate about. **Job Summary** Serve as the Scientist responsible for the development and execution of moderately complex testing and… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... colleagues while developing and expanding your career. The Director (Principal Scientist ) has primary responsibility for the planning and directing of clinical… more
- Charles River Laboratories (Wayne, PA)
- …above. * Certification/Licensure: None. * Other: Demonstrated knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries ... and troubleshoot laboratory experiments, tests, and procedures within accepted regulatory compliance for the characterization and analysis of biotherapeutics through… more
- Charles River Laboratories (Wayne, PA)
- …above. * Certification / Licensure: None * Other: Knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries is ... and troubleshoot laboratory experiments, test, and procedures within accepted regulatory compliance for the characterization and analysis of biotherapeutics through… more
- Merck (Upper Gwynedd, PA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The ** Senior Clinical Director (Sr. Principal Scientist )**...pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior … more