• Daiichi Sankyo, Inc. (Bernards, NJ)
    …and approvalsExtensive experience developing companion diagnostics and devices.Experience of drug development and drug regulatory procedures.Understanding ... of strategic and tactical role and deliverables of Global Regulatory Strategy in the Drug and Device...deliverables of Global Regulatory Strategy in the Drug and Device Development and Commercialization process.Experience with developing… more
    HireLifeScience (05/29/25)
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  • IQVIA, Inc. (Durham, NC)
    …Management (Associate) Director will play a critical role in supporting the Regulatory Affairs and Drug Development Solutions (RADDS) team-not through direct ... alignment to help drive success. This is role focuses on the Drug Development & Regulatory Strategy (DDRS) offerings within RADDS. The individual will be focused… more
    Upward (07/17/25)
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  • Merck & Co. (Rahway, NJ)
    …model-informed regulatory framework to impact strategies and decisions of drug discovery and development teams. Collaborate with other functional areas, as well ... of increasing responsibility and independence in a similar role in pharmaceutical drug development, regulatory agency, or academia. Educational background in… more
    HireLifeScience (07/19/25)
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  • Merck & Co. (Rahway, NJ)
    …Skills: Experience with sterile GMP facility startup.Knowledge of Investigational drug regulatory requirements.Understanding of Clinical Supply Chain ... (FLEx) Center is a new multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply… more
    HireLifeScience (07/11/25)
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  • Merck & Co. (North Wales, PA)
    …that include coordinating the activities of a programming team.US and/or worldwide drug or vaccine regulatory application submission experience at the leadership ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
    HireLifeScience (07/26/25)
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  • Merck & Co. (San Francisco, CA)
    drug discovery and development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within ... Pharmacokinetics, Pharmacology, Pharmacometrics, PKPD Modeling, Population Pharmacokinetics, R-Studio, TeamworkPreferred Skills: Drug Discovery Process, Global Regulatory , Machine Learning,… more
    HireLifeScience (07/12/25)
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  • Merck & Co. (North Wales, PA)
    …processes (SOPs) and software development life-cycle (SDLC) US and/or worldwide drug or vaccine regulatory application submission experience including the ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
    HireLifeScience (05/21/25)
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  • Merck & Co. (Boston, MA)
    drug discovery and development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within ... with ability to understand how MIDD can drive portfolio and regulatory decisionsDeep knowledge of drug development, pharmacokinetics and pharmacology… more
    HireLifeScience (07/12/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description:The Vice President, Regulatory Affairs, General Medicine, will contribute to the mission and vision of the Global Regulatory ... strategy with US FDA and global health authorities to advocate advanced regulatory strategies for novel medicines.Contributing to the continuous improvement of the… more
    HireLifeScience (07/04/25)
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  • Eisai, Inc (Nutley, NJ)
    …your profile, we want to hear from you. Job Summary The Executive Director, Regulatory Affairs will provide leadership and direction for the global regulatory ... under development and post approval research, including the development of regulatory strategies to ensure effective achievement of regulatory /business… more
    HireLifeScience (05/07/25)
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  • Merck & Co. (Rahway, NJ)
    …in cell culture commercialization. The primary objective of the Biologics Drug Substance Commercialization (BDSC), Cell Culture Sciences department is to provide ... process validation, second generation process development and authoring of regulatory submissions.-Under the general scientific and administrative direction of the… more
    HireLifeScience (07/17/25)
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  • Merck & Co. (Rahway, NJ)
    …process change requests and deviation reports while ensuring regulatory compliance.Education and Minimum Requirements:Bachelor's degree in engineering, chemistry ... Relationships, Lean Manufacturing, Manufacturing Processes, Manufacturing Support, Pharmaceutical Manufacturing, Regulatory Compliance, Root Cause Analysis (RCA), Stakeholder Engagement, Stakeholder… more
    HireLifeScience (07/25/25)
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  • Merck & Co. (Rahway, NJ)
    …high-volume clinical and commercial assembly equipment and processes for medical devices/ drug delivery systems. Reporting to the Director responsible for this area, ... equipment and processes for clinical and commercial manufacture of drug -device combination products.Hands on troubleshooting in a manufacturing environment with… more
    HireLifeScience (07/22/25)
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  • Merck & Co. (Rahway, NJ)
    …team is responsible for the research and development of sterile & parenteral drug products for biologics, Antibody Drug Conjugates and Small Molecules, including ... formulation, manufacturing process, and primary packaging to enable phase appropriate regulatory filings for large molecule sterile products. -These sterile products… more
    HireLifeScience (07/24/25)
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  • Merck & Co. (Rahway, NJ)
    …in late stages of development, and working collaboratively with receiving sites, drug product partners, and Technical Product Leaders, regulatory and ... and combination products, with a focus on autoinjectors, prefilled syringes, and other drug delivery systems. The director will lead a team of engineers and… more
    HireLifeScience (07/19/25)
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  • Merck & Co. (Rahway, NJ)
    …of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Director may be responsible ... of generating early clinical development plan and Investigational New Drug applicationsDeveloping of clinical development strategies for investigational or marketed… more
    HireLifeScience (07/26/25)
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  • Merck & Co. (North Wales, PA)
    …scientific leadership in design and analysis of clinical trials; Experience with regulatory filing for approval of drug /vaccine products; Prior experiences with ... design, computing software and data management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/… more
    HireLifeScience (07/15/25)
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  • Merck & Co. (South San Francisco, CA)
    …you passionate about leveraging cutting-edge AI/ML technologies to revolutionize drug discovery and development? The Pharmacokinetics, Dynamics, Metabolism, and ... AI/ML to support efforts in transforming the way PDMB leads the assessment of drug candidates. The successful candidate will join a dynamic Data Science team focused… more
    HireLifeScience (07/22/25)
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  • Genmab (NJ)
    drug development pertaining to statisticsExperience with the relevant regulatory requirements for biostatistics processes and SOPsExperience with regulatory ... scientific and technical progress within the field of biostatistics in drug development and advise of new methodologies that may support innovation… more
    HireLifeScience (07/03/25)
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  • 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 ... Responsibilities :Develops, coordinates, and provides biostatistical support for related drug /vaccine projects under supervision in Late Development Statistics. --Interacts… more
    HireLifeScience (07/16/25)
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