- 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
- Organon & Co. (Jersey City, NJ)
- …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 (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
- 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
- Burns & McDonnell (Morristown, NJ)
- **Description** Burns & McDonnell is seeking an Associate / Principal Engineer, Hydrogeologist, Scientist in a related field to join our successful team of ... capping, and other industry standard methods. + Strong working knowledge of regulatory frameworks, including CERCLA, RCRA, Section 401 and Section 404 permitting. +… more
