• Tris Pharma (Monmouth Junction, NJ)
    …Junction, New Jersey, Tris has an immediate opening for a QA R&D Senior ChemistSUMMARY:The Quality Assurance (QA) Research and Development (R&D) Senior Chemist ... with test method changes, component changes, qualification of alternate sourced drug substances)Performs testing for raw materials, packaging components, IP, FP… more
    HireLifeScience (04/30/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ... an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Sr . Manager of Operations - Continuous Improvement and Projects as part of the… more
    HireLifeScience (02/16/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on… more
    HireLifeScience (05/09/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Team (SMT) materials- Supports overall program safety reporting (eg, Periodic Safety Update Reports (PSURs), Drug Safety Update Reports (DSURs), ... Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical… more
    HireLifeScience (05/15/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …in R&D as early as possible. This led us to create the Translational Patient Safety Senior Director position, which will have unique exposure to Daiichi Sankyo's ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...senior leadership at DP0. Surface expert knowledge on safety biomarkers that might be used in preclinical and… more
    HireLifeScience (03/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... relevant stakeholdersPartners with cross-functional leaders incl. from across RD, Safety , Tech/Supply and Commercial to coordinate SMEs and engagement activities… more
    HireLifeScience (04/23/24)
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  • Catalent (St. Petersburg, FL)
    …organization. The QA Manager may oversee a staff from five to ten including Sr QA Technical Reviewers and QA Product Managers. Responsible for ensuring the site is ... and/or equivalent combination of education and experience as QA in pharmaceutical industries. Prior experience working with quality control, manufacturing, product… more
    HireLifeScience (05/04/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …generation, design and leadership of clinical development plans, and addressing all regulatory, drug and patient safety , data, CMC, IP, patient selection, market ... Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical… more
    HireLifeScience (05/10/24)
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  • Merck & Co. (Rahway, NJ)
    …managing budgets to align actions with strategy.Supervises 5 Directors or Senior Directors, and through them, approximately 85 scientists, people managers, chemical ... engineers, process safety , pilot plant operations and equipment development staff, and...for safe and compliant operations in the small molecule drug substance pilot plant facility, owning the automation control… more
    HireLifeScience (05/14/24)
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  • Insmed Incorporated (Bridgewater, NJ)
    …Millennials™ lists.OverviewThe Director, Toxicology, is a key member of the nonclinical safety team, reporting to the Executive Director, Head of Toxicology and ... you will represent toxicology at cross-functional project teams, strategize nonclinical safety data package, oversee safety pharmacology and toxicology studies,… more
    HireLifeScience (03/12/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ... for the investigations management system. Working closely with the Quality Senior Manager, this position will ensure alignment with all applicable regulations… more
    HireLifeScience (04/19/24)
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  • Bering Straits Native Corporation (Jamestown, ND)
    …System (RMS). Include comments and monitoring of progress, work activities, safety issues and subcontractor manpower in the reports. Responsibilities ESSENTIAL ... functions. Required (Minimum Necessary) Qualifications (applies to both this section and KSAO's) Senior Scheduler must have at least ten (10) years of experience… more
    JobGet (05/14/24)
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  • Option Care Health (Nashville, TN)
    …provide counseling to home care patients and/or their caregivers.Ensures continuity of pharmaceutical care to and from the home and other patient-care settings. Uses ... without incompatibilities, stable, and appropriately stored. Adheres to appropriate safety and quality assurance practices. Prepares labels that conform to… more
    JobGet (05/15/24)
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  • Integrated Resources, Inc (Rahway, NJ)
    …Duration: 12 months Job Description: * Conducts release and stability testing of drug products following SOPs and cGMPs. * Plans and executes validation of ... adapt methods. * Solves more complex problems with some guidance from senior scientists. * Troubleshoots instrumentation. * May investigate new technologies. *… more
    JobGet (05/03/24)
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  • Sr Manager, Drug Safety Data

    Mitsubishi Chemical Group (Jersey City, NJ)
    …researching on real-world evidence, and creating hope for all facing illness. Manages Drug Safety Data Systems to ensure the timely creation, deployment and ... maintenance of databases required by MTDA Drug Safety projects. Analyzes study protocol and...a combination of education and experience + 8+ years pharmaceutical experience in clinical and/or safety setting… more
    Mitsubishi Chemical Group (04/21/24)
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  • Engineering Projects Sr Mgr

    Amgen (New Albany, OH)
    …Engineering or Scientific experience **Preferred Qualifications:** + Experience leading Pharmaceutical / Biotechnology projects, preferably Packaging and/or Drug ... a career you can be proud of. Engineering Projects Sr Mgr **Live** **What you will do** Let's do...Global Strategic Sourcing, Project Controls Services, Environmental Health and Safety , Global Asset Planning, Finance and Strategy, Law, and… more
    Amgen (02/25/24)
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  • Open Rank-Instructor, Sr . Instructor-…

    University of Colorado (Aurora, CO)
    Open Rank-Instructor, Sr . Instructor- Clinical APP - 33036 Faculty **Description** **University of Colorado Anschutz Medical Campus** **Department: Pediatrics, ... Section of Infectious Disease** **Job Title:** **Open Rank-Instructor, Sr . Instructor** **Position #00773460: - Requisition #:33036** **Job Summary:** Key… more
    University of Colorado (03/23/24)
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  • Sr . Pharmacy Buyer - Charge Analyst

    University of Miami (Miami, FL)
    …. Sr . Buyer - Charge Analyst POSITION SUMMARY: The Senior Buyer - Charge Analyst will direct procurement activities, supply management and ... medication formulary list and charge description maintenance, which include timely drug addition/deletion, coding and pricing updates + Completes Pharmacy Work… more
    University of Miami (05/15/24)
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  • Sr Principal/Principal Scientist, In Vivo…

    Boehringer Ingelheim (Ridgefield, CT)
    …+ PhD in Immunology or related discipline with at least 7 years drug discovery experience in pharmaceutical industry or biotech or equivalent and, ... Requirements:** + PhD in Immunology or related discipline with at least 5 years drug discovery experience in pharmaceutical industry or biotech and, at least, 2… more
    Boehringer Ingelheim (04/30/24)
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  • Sr . Clinical Development Medical Director

    System One (King Of Prussia, PA)
    …of education and experience Experience/The Ideal for Successful Entry into Job: + Drug development experience in biotechnology or pharmaceutical industry, or a ... Title: Sr . Clinical Development Medical Director Location: Must be...research studies. Responsibilities also include adverse event reporting and safety responsibilities monitoring. Monitors adherence to protocols and determines… more
    System One (05/13/24)
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