- Organon & Co. (Plymouth Meeting, PA)
- …**The Position ** Reporting to the Director in Organon Regulatory CMC, the Associate Principal Scientist is responsible for developing and implementing ... with global regulations and guidance, and Organon procedures. The Associate Principal Scientist will lead...products and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for… more
- Merck (West Point, PA)
- Job Description Associate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent) Our company's Device Product & ... ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead… more
- Humana (Harrisburg, PA)
- …us in shaping the future of healthcare through AI excellence. We are seeking a Principal Data Scientist to guide the strategic decisions and the development of ... the healthcare sector, specifically Medicare Advantage, and an understanding of regulatory frameworks and market dynamics. Advanced Technical Skills : Experience… more
- Organon & Co. (Plymouth Meeting, PA)
- …Director in Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the Associate Principal Scientist is responsible for developing and ... with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead...products and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.… more
- Merck (West Point, PA)
- **Job Description** ** Associate Principal Scientist - Downstream Vaccines and Advanced Biotechnologies Process R&D** Vaccines and Advanced Biotechnologies ... and Clinical Supply Manufacturing. We are seeking an innovative, highly motivated, and experienced Associate Principal Scientist to join us at our research… more
- Merck (West Point, PA)
- **Job Description** ** Associate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent)** _Our company's Device ... ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead… more
- Merck (West Point, PA)
- …Description** We are seeking a motivated and experienced Translational PET Imaging Scientist to lead the transition of novel PET radiotracers from late preclinical ... on clinical implementation of novel PET tracers in oncology studies, guide regulatory submissions, and act as the PET imaging expert within multidisciplinary project… more
- Merck (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… more
- Merck (Upper Gwynedd, PA)
- **Job Description** The **Clinical Director ( Principal Scientist )** has primary responsibility for the strategic planning and directing clinical research ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May Be… more
