- 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)
- …therapeutic areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition ... the clinical instruction(s) and commercial market approval(s) of combination products. Principal ResponsibilitiesLead, set direction, align with key stakeholders, and… 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. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be… more
- Organon & Co. (Jersey City, NJ)
- …to the Director or Executive Director in Organon Regulatory CMC, the Associate Principal Scientist is responsible for developing and implementing ... 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)
- …areas and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will lead the definition and ... clinical instruction(s) and commercial market approval(s) of combination products. ** Principal Responsibilities** + Lead, set direction, align with key stakeholders,… 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 ... 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
- Pfizer (Pearl River, NY)
- …and publications. + May contribute budget execution of protocols. **Interact with regulatory authorities, key opinion leaders, and principal investigators** + ... set within a matrix team in executing studies, performing medical monitoring, supporting regulatory interaction, and taking on a leadership role in study teams for… more
- Merck (Rahway, NJ)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May… 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
