- 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
- 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 ... products in accordance with global regulations and?guidance, and?Organon procedures.? The Associate Principal Scientist will lead the?preparation and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJOB DESCRIPTION SUMMARY Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary ... clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products....studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the… more
- Merck & Co. (Rahway, NJ)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... Real-World Evidence (RWE) Capabilities & Analytics team is looking for an Associate Director, Data Strategy & Partnerships with expertise in data strategy, advanced… more
- Merck & Co. (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions.-We are seeking a strategic and technical leader with ... Provide technical oversight of cell culture process development, process characterization and regulatory filing activities to ensure a smooth and clear path to… more
- Merck & Co. (Rahway, NJ)
- …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 & Co. (North Wales, PA)
- …span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.-Design and maintain statistical ... and systems and database expertise;US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
- Merck (Rahway, NJ)
- …Description** **JOB DESCRIPTION SUMMARY** _Primary activities include but are not limited to:_ The Associate Principal Scientist is a DVM and/or PhD whose ... clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products....studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the… more
- Charles River Laboratories (Ashland, OH)
- …Ensure scientific Integrity of studies, with minimal oversight. * Function as a Principal Investigator, Individual Scientist , and/or Project Scientist as ... a career that you can feel passionate about. **Job Summary** Serve as a scientist in the conduct of assigned nonclinical research studies of basic complexity, to… more
- Merck (South San Francisco, CA)
- …The SSF Pharmacokinetics, Dynamics, Metabolism and Bioanalytics (PDMB) group is seeking an Associate Principal Scientist to contribute to our Company's ... biologics, drug conjugates, and novel modality discovery and development pipeline. The Associate Principal Scientist will be primarily discovery team-facing… more
- Amgen (South San Francisco, CA)
- …Join us and transform the lives of patients while transforming your career. ** Principal Scientist - Clinical Pharmacology, Modeling & Simulation** **What you ... Modeling & Simulation Department at Amgen is seeking a Principal Scientist . In this vital role, you...of Clinical Pharmacology and Modeling & Simulation experience **Or** Associate 's degree and 10 years of Clinical Pharmacology and… more
- Unilever (El Segundo, CA)
- …thinker to join our dynamic team at Liquid IV Quality Assurance Department as Associate Principial QA Scientist , focusing on the analysis and interpretation of ... efficiency, sensitivity, and/or cost improvement as well as following regulatory requirements. **Qualifications:** The successful candidate will have the following… more
- Merck (Rahway, NJ)
- …investigations, process validation, second generation process development and authoring of regulatory submissions. We are seeking a strategic and technical leader ... Provide technical oversight of cell culture process development, process characterization and regulatory filing activities to ensure a smooth and clear path to… more
- Merck (Rahway, NJ)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... Real-World Evidence (RWE) Capabilities & Analytics team is looking for an Associate Director, Data Strategy & Partnerships with expertise in data strategy, advanced… more
- Merck (Rahway, NJ)
- …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 (North Wales, PA)
- …the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. + Design and maintain ... systems and database expertise; + US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
- Amgen (Washington, DC)
- …us and transform the lives of patients while transforming your career. **Senior Principal Scientist - Global Diagnostic Development Lead** **What you will do** ... assay to marketed Diagnostic to support the clinical development strategy for regulatory approval and commercialization. As such, the Dx group works closely with… more
- Walmart (Bentonville, AR)
- …service operations and technology solutions for Finance, People, and the Associate Digital Experience. **About People.AI Team** The People.AI team is responsible ... intelligent experience within a chatbot or business application to enhance associate experience and productivity. You will design and build an intelligent… more
- Charles River Laboratories (Mattawan, MI)
- …Ensure scientific integrity of studies with minimal oversight + Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with ... and quality observations + Assist in problem solving for technical and/or regulatory issues with oversight + Responsible for writing and preparing study… more
- Charles River Laboratories (Mattawan, MI)
- …scientific integrity of studies with minimal oversight. + Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with ... and quality observations. + Assist in problem solving for technical and/or regulatory issues with oversight. + Responsible for writing and preparing study… more
