- Organon & Co. (Jersey City, NJ)
- …project teams and alliance partners to develop and implement world-wide regulatory strategies for assigned biosimilar projects, with a specific focus on ... Regulatory CMC (Chemistry, Manufacturing, and Controls) requirements. This role...development due diligence activities. **Responsibilities** + Provide global strategic regulatory CMC overview for respective products and portfolio. +… more
- Merck (Rahway, NJ)
- **Job Description** **JOB DESCRIPTION SUMMARY** The Associate Principal Scientist is a DVM/VMD and/or PhD whose primary function is to design, coordinate, ... 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)
- **Job Description** ** Associate Principal Scientist , Biologics Analytical Research & Development** Our Research Scientists are our Inventors. We identify and ... department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Rahway, New… more
- Merck (Rahway, NJ)
- **Job Description** **Container Closure Integrity Testing Lead, Associate Principal Scientist , Analytical Research & Development** The Analytical Research ... and Development group has an opening for an Associate Principal Scientist based in...external sites and be familiar with current industry and regulatory requirements on CCIT. This position will involve method… more
- Merck (Rahway, NJ)
- …Cell Based Sciences team in Rahway, NJ is seeking a motivated scientist with technical expertise in **Biologics Potency** assays in drug **Development** . ... context of broader process and product development. + Working knowledge of regulatory guidance and quality standards, with experience authoring and reviewing … more
- Merck (Rahway, NJ)
- **Job Description** **Senior Principal Scientist , Precision Medicine, Immunology** Precision Medicine is an integral part of our Immunology Therapeutic Area. To ... aligned with the Precision Medicine goals for relevant programs/assets The Senior Principal Scientist is responsible for maintaining a strong scientific fund… more
- Merck (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions. Under the general scientific and administrative direction of ... next generation process development and characterization, process validation, and regulatory submission authoring **In this role, the successful candidate will… 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 (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