- Merck & Co. (Rahway, NJ)
- Job DescriptionJOB DESCRIPTION SUMMARYThe Associate Principal Scientist is a DVM/VMD and/or PhD whose primary function is to design, coordinate, monitor, and ... Good Clinical Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies.The Associate Principal Scientist is the primary clinical study… more
- Merck & Co. (Rahway, NJ)
- …department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Rahway, New ... Jersey research facility.- The Associate Principal Scientist is a...molecular biology and immunoassay techniques.Extensive knowledge and experience with regulatory guidance and industrial standards of control strategy for… more
- Merck & Co. (Rahway, NJ)
- …DescriptionAn excellent opportunity is available for an Analytical Research and Development (AR&D) Associate Principal Scientist to serve as a Device ... GMP labs and commercial QC labsPartner with cross-functional device, analytical, regulatory and quality functions within our divisions to manage End-to-End MDCP… 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)
- …department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Rahway, New ... Jersey research facility.- The Associate Principal Scientist is a...program deadlines.Authoring and reviewing internal technical reports, sections of regulatory filings (eg, IND, BLA) and external scientific publications.Experience… more
- Merck & Co. (Rahway, NJ)
- …responsive supply.The individual will have a deep understanding of the global regulatory and business environment and the needs related to pharmaceutical drug ... development and commercializationWorking knowledge of CMC filing requirements and regulatory guidances (eg, ICH) for drug substance and/or drug productExperience… more
- Merck & Co. (Rahway, NJ)
- … regulatory submissions. -Under the general scientific and administrative direction of Associate Principal Scientist , and working in conjunction with ... and trend evaluations, process characterization, new WCB qualification, and regulatory submission authoring, with a focus on standardization across programs.In… more
- Merck & Co. (Rahway, NJ)
- … regulatory submissions. -Under the general scientific and administrative direction of Associate Principal Scientist , and working in conjunction with ... Biological, Chemical, Automation, Safety, Technical Services, Process Development, Analytical, Regulatory , and Quality.As part of Our Company's Manufacturing Division,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist / Associate Director, has primary responsibility for ... reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programsIn collaboration… 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
- L'Oreal USA (Clark, NJ)
- …(https://careers.loreal.com/en\_US/content/Home) / Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 206467 Associate Principal Clinical Research ... Jersey Clark, NJ Research & Innovation Full - Time 27-May-2025 Position Title: Associate Principal Clinical Research Scientist , Open Clinical Innovation… 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)
- …department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Rahway, New ... Jersey research facility. The Associate Principal Scientist is a...+ Authoring and reviewing internal technical reports, sections of regulatory filings (eg, IND, BLA) and external scientific publications.… more
- Merck (Rahway, NJ)
- …An excellent opportunity is available for an Analytical Research and Development (AR&D) Associate Principal Scientist to serve as a Device Analytical ... labs and commercial QC labs + Partner with cross-functional device, analytical, regulatory and quality functions within our divisions to manage End-to-End MDCP… 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)
- …supply. + The individual will have a deep understanding of the global regulatory and business environment and the needs related to pharmaceutical drug substance and ... development and commercialization + Working knowledge of CMC filing requirements and regulatory guidances (eg, ICH) for drug substance and/or drug product +… more
- Merck (Rahway, NJ)
- … regulatory submissions. Under the general scientific and administrative direction of Associate Principal Scientist , and working in conjunction with ... and trend evaluations, process characterization, new WCB qualification, and regulatory submission authoring, with a focus on standardization across programs.… more
- Merck (Rahway, NJ)
- … regulatory submissions. Under the general scientific and administrative direction of Associate Principal Scientist , and working in conjunction with ... Biological, Chemical, Automation, Safety, Technical Services, Process Development, Analytical, Regulatory , and Quality. As part of Our Company's Manufacturing… more
- Merck (Rahway, NJ)
- …Description** **Role Summary** + Under the guidance of a senior leader, an Associate Principal Scientist / Associate Director, has primary responsibility ... barriers to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programs + In… more
