- Merck & Co. (North Wales, PA)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... dedicated colleagues while developing and expanding your career.-- Director (Principal Scientist ) has primary responsibility for the planning and directing of… more
- Merck (North Wales, PA)
- **Job Description** We are seeking a Senior Director (Sr. Principal Scientist ) Global Regulatory Affairs Liaison with a visionary, growth-oriented ... priorities. **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible for development and implementation… more
- 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 (Upper Gwynedd, PA)
- **Job Description** We are seeking a Director (Principal Scientist ), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... pipeline and drive our strategic priorities. The Director, Principal Scientist | Regulatory Affairs Liaison...+ Reports to Associate Vice President, Executive Director, or Senior Director in the General Medicine Therapeutic Area. +… more
- J&J Family of Companies (Spring House, PA)
- Associate Director, CMC Regulatory Affairs + Job titleAssociate Director, CMC Regulatory Affairs + FunctionDiscovery & Pre-Clinical/Clinical Development ... + Sub functionRegulatory Science + CategorySenior Principal Scientist , Regulatory Science (ST8) + LocationHorsham, Pennsylvania,...& Johnson is recruiting for an Associate Director, CMC Regulatory Affairs . This position can be located… 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
- 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
- J&J Family of Companies (Titusville, NJ)
- …quality monitoring & compliance, data management, global medical safety, biostatistics, regulatory affairs , clinical supplies unit, medical writing, clinical ... Data Monitoring Committee (IDMC) and adjudication meetings as needed + Assists Regulatory Affairs in determining requirements for any corrective actions or… more
- J&J Family of Companies (Horsham, PA)
- …medical affairs including collaborating closely with compliance, privacy, and regulatory partners + Build scalable analytics solutions in partnership with Data ... Analytics & Computational Sciences + Sub functionData Science + CategoryPrincipal Scientist , Data Science (ST7) + LocationTitusville, New Jersey, United States;… more
