- CHRISTUS Health (Winnsboro, TX)
- …CORE values of CHRISTUS Health. Must complete all required compliance and regulatory tasks and follow all applicable policies and procedures. Performs other duties ... as assigned. Job Requirements: Education/Skills Bachelor's Degree or higher in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution or equivalent laboratory training and experience meeting the… more
- Merck & Co. (Rahway, NJ)
- Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for ... point in the drug development process, working closely with scientific, regulatory , statistical, and modelling colleagues across the organization to translate the… more
- Merck & Co. (Rahway, NJ)
- …in Development and Supply (ACDS) is seeking applicants for an Associate Principal Scientist position available at the Rahway, NJ and West Point, PA sites.-The ... pharmaceutical drug product development and commercialization. The Associate Principal Scientist responsibilities include, but not limited to, analytical method… more
- Merck & Co. (Rahway, NJ)
- …SUMMARY Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary function is to design, coordinate, ... and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products. The position requires… more
- Merck & Co. (North Wales, PA)
- …highly motivated and experienced Anatomic Pathologist (MD) for the role of Principal Scientist (Director) to join our innovative team. This position will play a ... digital pathology within our company's clinical therapeutic pipeline.The Principal Scientist (Director) will have the following responsibilities: Engage in providing… more
- Merck & Co. (Rahway, NJ)
- Job Description Sr. Scientist , Small Molecule Analytical Research & Development The Small Molecule Analytical Research and Development group has an opening for a ... Senior Scientist based in Rahway, NJ. Join us and experience...tools, and data analysis. You will also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Principal Scientist , Drug Discovery in our Research and Development Department will be responsible for identifying new molecular entities and ... Safety & Toxicology).- The position will report directly to the Distinguished Scientist and Global Head, our Company's Research & Development Liaison and Discovery… more
- Merck & Co. (Rahway, NJ)
- …Biologics Process Research & Development (BPR&D) as a Senior Principal Scientist .BPR&D within Research Laboratories is committed to rapidly delivering diverse ... with the scientific community to influence the field.As a Senior Principal Scientist , you will drive various strategic initiatives and translate strategies into-… more
- Aequor (Thousand Oaks, CA)
- …candidates.The Department of Oncology Research is seeking a highly motivated Scientist to contribute to the discovery and progression of small-molecule therapeutics. ... and experimental difficulties. Contributes to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions and/or patents. Participates in… more
- Merck & Co. (Rahway, NJ)
- …Analytical Commercialization Technology group currently has an exciting opportunity for a Scientist at our Rahway, NJ site. The position is a laboratory-based ... development and validationStability testingContribute to relevant analytical sections of regulatory submissionsYou'll have the opportunity to work with teams… more
- Merck & Co. (Rahway, NJ)
- …of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of design verification ... Company and with external partners.Author and review relevant portions of the regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for combination product programs… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are seeking a highly motivated Senior Scientist to join our Biologics Potency team within the Cell-Based Sciences, Analytical Research and ... accurate and detailed laboratory records.Contribute to the preparation of regulatory submissions and technical reports.Education: Ph.D. in Cell Biology,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are seeking a highly experienced and skilled Distinguished Scientist to join our Device Development & Technology (DD&T) organization to serve as a ... medical device engineering, particularly in the design, manufacturing, and regulatory aspects of Autoinjectors and combination products.Primary Responsibilities:Technical Strategic… 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)
- …of our Research & Development Division is seeking applicants for a Senior Scientist position available at its Rahway, New Jersey research facility. The Senior ... Scientist is a laboratory-based scientific role tasked with solving...program deadlines.Authoring and reviewing internal technical reports, sections of regulatory filings (eg, IND, BLA) and external scientific publications.Strong… more
- Merck & Co. (South San Francisco, CA)
- …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 and is expected to be a key contributor to the… more
- BioAgilytix (Durham, NC)
- …life-saving therapeutics to the patients who need them.We are seeking a Scientist I/II to join our LC/MS large molecule team, supporting bioanalytical studies ... in alignment with GLP requirements. This is an excellent opportunity for a scientist with hands-on LC/MS experience who is looking to deepen their expertise in… 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 ... dataProduce tables and graphics for inclusion in study reports and regulatory submissionsEnsure programmatic traceability from data source to modeling resultSupport… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Description This position is for a principal scientist in biostatistics.-The candidate should have a solid knowledge of statistical ... design, computing software and data management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/… more
- Eisai, Inc (Exton, PA)
- …CAPAs.Help in the administration of external stability programs, ensuring regulatory compliance, adherence to protocol requirements and timely completion of ... and maintain SOPs, forms, protocols and other controlled documents.Draft regulatory documents to support IND/IMPD/BLA/MAA filings.Present assay/stability study results… more
