• Pharmaceutical Change Control Process Owner

    Bausch Health (Bridgewater, NJ)
    …for data collection for quality metrics, scorecards, and quality review board meetings. + Lead internal audits, support regulatory inspections, address audit ... Join our global diversified pharmaceutical company enriching lives through our relentless drive...the electronic quality management system (RemarQue) and ensure timely review and closure. + Collaborate with CMOs and cross-functional… more
    Bausch Health (07/31/25)
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  • Senior Manager, MS&T Mseo Manufacturing Systems…

    Bristol Myers Squibb (Summit, NJ)
    …MSAT Manufacturing Systems Engineering and Operations Manufacturing Systems Automation and Data Analytics Engineer is accountable for leading activities and assigned ... resources responsible for Data Analytics solutions and insights (SQL, Azure AI, Phyton...it. + Working knowledge of Electronic Batch Records (EBR), Review by Exception (RBE), and MES Recipe object lifecycle… more
    Bristol Myers Squibb (07/18/25)
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  • Data Scientist, Operations Research

    Cardinal Health (Trenton, NJ)
    **_What Data Science contributes to Cardinal Health_** The Data and Analytics Function oversees the analytics life-cycle in order to identify, analyze and ... to achieve a competitive advantage. This function manages analytic data platforms, the access, design and implementation of reporting/business intelligence… more
    Cardinal Health (07/18/25)
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  • Senior Manager, Clinical Data Standards

    Bristol Myers Squibb (Princeton, NJ)
    …of post-baccalaureate experience. Must have experience with/in: + Clinical Trial Data , + Pharmaceutical development process, + Health Authority regulations, ... personal lives. Read more: careers.bms.com/working-with-us . **Senior Manager, Clinical Data Standards, Bristol-Myers Squibb Company** **,** **Princeton, NJ** **.**… more
    Bristol Myers Squibb (07/16/25)
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  • Director, Sterile Product Development

    Merck (Rahway, NJ)
    …concepts, tools, and requirements for all dosage forms (liquid, lyo, drug-device combinations) + Review and approval of data and technical documents + Ability to ... This research opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development… more
    Merck (07/24/25)
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  • Director, Regulatory Affairs

    Bausch Health (Bridgewater, NJ)
    Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it ... of the product development team to provide regulatory guidance for pharmaceutical products. Manages relevant regulatory strategy components and interactions with… more
    Bausch Health (07/01/25)
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  • Sr Manager, Incentive Compensation

    Mitsubishi Chemical Group (Jersey City, NJ)
    …in successfully managing incentive compensation programs. + Possess deep knowledge of pharmaceutical data , including IQVIA Xponent, activity data , and ... company - one of Japan's most respected - is a research-driven pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. MTPC… more
    Mitsubishi Chemical Group (05/31/25)
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  • Scientist

    Kelly Services (New Brunswick, NJ)
    …to internal SOPs and USP monographs. Report data accurately and promptly. + ** Data Review and Trending:** Conduct peer data reviews and analyze ... **Job Title:** QC Scientist - Pharmaceutical Manufacturing Support **Job Summary:** The primary responsibilities...troubleshoot and calibrate equipment as needed. + Knowledge of data review processes, trending, and documentation of… more
    Kelly Services (07/19/25)
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  • Associate Medical Director, PVRM

    Sumitomo Pharma (Trenton, NJ)
    …specific and/or clinical study team meetings and governance committees. + Performs aggregate review of post-marketing safety data in support of safety signal ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations...trials, including monitoring of clinical trial safety and laboratory data . + Generates safety queries, evaluates safety data more
    Sumitomo Pharma (08/02/25)
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  • Associate Principal Scientist (Associate Director)…

    Merck (Rahway, NJ)
    …to the Sr Director/Director/Principal Scientist/Sr Principal Scientist in Pre-approval Pharmaceutical CMC is responsible for developing and implementing CMC ... regulatory strategies for our company's pharmaceutical pipeline products in accordance with global regulations and...risks. + Lead the development, communication, lifecycle management and review of the CMC Regulatory Strategy Document for assigned… more
    Merck (07/19/25)
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