- Merck & Co. (Rahway, NJ)
- …energetic individual to join our Biologics Process Development Department as an Associate Principal Scientist .- Applicant must have effective organizational ... scalable cell culture processes.Responsible for process development, process characterization, and regulatory filing activities to ensure a smooth and clear path to… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionOur company's Research Laboratories in South San Francisco is seeking an Associate Principal Scientist with strong expertise in translational ... analysis, and reporting to project teams, governance bodies, and regulatory agencies.Drive scientific innovation and champion new enabling technologies and… more
- Insmed Incorporated (San Diego, CA)
- …Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Assistant Principal Scientist will be a part of a multidisciplinary team ... engineering cell lines (knock out/knock in) for potency bioassay. The Assoc. Principal Scientist will develop, improve, implement, transfer and co-validate… more
- Merck & Co. (North Wales, PA)
- …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 Clinical Director ( Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research activities ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Clinical Director May Be… more
- Aequor (Thousand Oaks, CA)
- …to work in a dynamic team-based culture. This position reports to a Principal Scientist in TS&BA. Role Responsibilities Confirm the accuracy of experimental ... to support the quality control/review of nonclinical scientific reports. Title: Associate Research Operations, Nonclinical Report QC As part of the Translational… more
- Merck & Co. (Rahway, NJ)
- …department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, 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 (West Point, PA)
- …growing pipeline of diverse products and evolving technologies. We are seeking an Associate Principal Scientist to advance and commercialize the intravitreal ... to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The...As a member of the drug product team, the Associate Principal Scientist will be… more
- Merck (Rahway, NJ)
- …biologics, and pharmaceutical products and combination products. We are seeking an experienced Associate Principal Scientist to advance and commercialize an ... to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The...a member of the ADC drug product team, the Associate Principal Scientist will have… more
- Merck (Rahway, NJ)
- …knowledge in both analytical experimental design and biotherapeutic pipeline programs. Finally, this Associate Principal Scientist will be a partner in ... Mass Spectrometry -group in Rahway, NJ is seeking a motivated scientist with technical expertise in mass spectrometry-based protein characterization. This position… more
- Merck (Rahway, NJ)
- …energetic individual to join our Biologics Process Development Department as an Associate Principal Scientist . Applicant must have effective organizational ... cell culture processes. + Responsible for process development, process characterization, and regulatory filing activities to ensure a smooth and clear path to… more
- Merck (West Point, PA)
- …and Clinical Supply Manufacturing. We are seeking an innovative, highly motivated, and experienced Associate Principal Scientist to join us at our research ... small technical development teams + Experience in authoring and reviewing CMC regulatory documentation The successful candidate will be expected to demonstrate the… more
- Merck (West Point, PA)
- …a healthier future for all. We have an exciting opportunity for an ** Associate ** ** Principal Scientist ** with significant experience in immunological assays ... professional development. + Properly document protocols and findings, author preclinical regulatory documents, and comply with all laboratory safety requirements. +… more
- Merck (South San Francisco, CA)
- …Description** Our company's Research Laboratories in South San Francisco is seeking an Associate Principal Scientist with strong expertise in translational ... generation, analysis, and reporting to project teams, governance bodies, and regulatory agencies. + Drive scientific innovation and champion new enabling… more
- Merck (West Point, PA)
- …process enhancements, next generation process development, and authoring of regulatory submissions. Under the general scientific and administrative direction of ... functional area on cross-functional and cross-divisional teams. + Authors required regulatory and technical documentation. Ensures that processes are developed and… 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 (San Diego, CA)
- **Job Description** The **Clinical Director ( Principal Scientist )** has primary responsibility for the strategic planning and directing clinical research ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May Be… 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 Kenilworth, New… more
- Lilly (Pleasant Prairie, WI)
- …for this position is $63,000 - $165,000 **Responsibilities:** The Sterility Assurance Scientist is a technical role that assists in development and implementation of ... gowning/aseptic techniques, and cleaning/sanitization strategies, including disinfectant efficacy. The principal role is a position that develops and implements a… more
- Merck (West Point, PA)
- **Job Description** **Job Title:** ** Associate Principal Scientist , Cell Culture and Fermentation Sciences Level: R4 (Research Path)** **Level:** **P4 ... manufacturing sites, manufacturing investigations, process validation, and authoring of regulatory submissions. Under the general scientific and administrative direction… more
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