- Fidelity TalentSource LLC (Boston, MA)
- Job Description: Principal Data Scientist , Fraud ManagementFidelity's Financial Intelligence Unit (FIU) is seeking an experienced, highly motivated data ... scientist with a passion for analyzing data in a...offsite with maximizing time together in person to meet associate and business needs. Currently, most hybrid roles require… more
- Fidelity TalentSource LLC (Boston, MA)
- Job Description:VP Data Science GenAIThe Role You are a seasoned scientist with a deep understanding of GenAI, and a burning desire to unlock its mysteries in the ... earnings notes, spreadsheet models, prospectuses, loan indentures, news reports, regulatory filings. It will support the deployment of personalized assistants… more
- L'Oreal USA (Clark, NJ)
- …(https://careers.loreal.com/en\_US/content/Home) / Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 187395 Associate Principal Scientist , ... Research & Innovation Full - Time 22-Aug-2024 Position Title: Associate Principal Scientist , Cosmetics Product...New Jersey (Hybrid) Department : Product Safety, SRCM (Safety, Regulatory , Claims, & Microbiology) For more than one hundred… more
- Merck (West Point, PA)
- **Job Description** **Position Description:** ** Associate Principal Scientist , Sterile Drug Product Commercialization** As part of Our Company's ... biologics, and pharmaceutical products and combination products. We are seeking an experienced Associate Principal Scientist to advance and commercialize a… more
- Merck (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...+ Authoring and reviewing internal technical reports, sections of regulatory filings (eg, IND, BLA) and external scientific publications.… more
- Merck (Rahway, NJ)
- **Job Description** **Position Description:** **Device Development Associate Principal Scientist - Development Strategy, Design Controls and Risk ... to ensure they are developed and manufactured in accordance with regulatory , company, and customer requirements. ** Principal Responsibilities** + Lead/contribute… more
- Merck (West Point, PA)
- **Job Description** Associate Principal Scientist to support mutagenic and non-mutagenic risk assessment activities as well as perform in silico assessments ... group within the Nonclinical Drug Safety organization is seeking an office-based scientist with expertise in impurity risk assessment. A core responsibility will be… more
- Merck (Lower Gwynedd, PA)
- …while developing and expanding your career. We are seeking a highly motivated Associate Principal Scientist to join the Department of Pharmacokinetics, ... assay development, qualification/validation, technology transfer, and/or troubleshooting to meet regulatory expectations for validation and line of sight for… more
- Merck (Rahway, NJ)
- …assays that are deployed in support of clinical trials. The candidate for this Associate Principal Scientist position should have strong technical expertise ... validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials.… more
- Merck (West Point, PA)
- …create a healthier future for all. We have an exciting opportunity for an ** Associate ** ** Principal Scientist ** with experience in Vaccine biology or ... professional development. + Properly document protocols and findings, author preclinical regulatory documents, and comply with all laboratory safety requirements. +… more
- Bristol Myers Squibb (Summit, NJ)
- …difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be part of the late stage TM ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… 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 (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... projects in Late Development Statistics. + Interacts with Clinical, Regulatory , Statistical Programming, Data Management, and other company Research Laboratories… more
- Dartmouth Health (Lebanon, NH)
- Overview FOR ADMINISTRATIVE PURPOSES ONLY - APPLICANT PREVIOUSLY IDENTIFIED Principal Scientist Psychiatry Research The Principal Scientist independently ... major contributions of substantive and original peer-reviewed work. * Acts as Principal Investigator. * Responsible or accountable for multiple grants and research… more
- AbbVie (North Chicago, IL)
- …strategies for the Analytical R&D (ARD) functions guided by global regulatory requirements, while effectively managing local and global interfaces across Small ... Molecule and Biologics Analytical R&D functions (SMARD/BARD), CMC Regulatory Affairs (RA), Quality Assurance (QA), CMC Coordination, Product Development Science and… more
- Bristol Myers Squibb (Cambridge, MA)
- …. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage TM group. The ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… more
- Merck (Rahway, NJ)
- …in compliance with departmental and company Standard Operating Procedures, regulatory requirements, and standards. **Primary Activities** **:** + Business System ... processes, assuring they are of high quality and complaint with regulatory requirements **Skills** **Education and Minimum Requirement** **:** + BA/BS in… more
- Merck (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
- Bristol Myers Squibb (New Brunswick, NJ)
- …every treatment we pioneer. Join us and make a difference. Position Summary The Principal Process Engineer/ Scientist acts as a technology transfer lead in the ... cGMPs, BMS procedures, and that processes are defined consistent with regulatory filings. This position must comply with all Security guidelines, Environmental… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …in different animal models, strong understanding of ethical and regulatory guidelines, project management skills, leadership experience, ability to collaborate ... a complex nature, assimilating information across functional areas, suitable for regulatory submission or external publication. + Directs resources in the… more
