• Acadia Pharmaceuticals Inc. (Princeton, NJ)
    …work in our office three days per week on average. Position Summary: The Associate Director (AD), Clinical Trial Materials (CTM) plays a pivotal role in the success ... programs across Phase I-IV and investigator-initiated studies (IIS). Reporting to the Sr . Director of Clinical Trial Materials, this strategic and hands-on leader is… more
    Upward (07/06/25)
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  • AD/ SR AD, US Product Group RA, US RRL…

    Boehringer Ingelheim (Ridgefield, CT)
    …for the Associate Director role and between $170,000 and $269,000 for the SR Associate Director role. The position may be eligible for a role specific ... Ph.D., Master's) preferred + Specialized Pharmacist or Master of Drug Regulatory Affairs, RAC certification preferred ** Associate Director Experience… more
    Boehringer Ingelheim (05/09/25)
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  • Sr Manager Engineering - Pre-Filled Syringe…

    Amgen (Thousand Oaks, CA)
    …Chain organizations) + Consider platform boundaries across operations, commercial, and regulatory labeling + Support appropriate prioritizing of programs, ... assess the lifecycle of pre-filled syringe devices to ensure post-market performance and regulatory compliance. Furthermore, the Senior Manager will play a key… more
    Amgen (07/15/25)
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  • SR AD / Director, Pharmacometrics (Remote)

    Boehringer Ingelheim (Ridgefield, CT)
    …your influence and deepening your knowledge in pharmacometric approaches? _The Senior Associate Director/ Director - Pharmacometrics will independently perform ... data science fields, clinical pharmacology, clinical drug development, MID3, and regulatory guidelines **Compensation:** This position, Sr . AD, Pharmacometrics,… more
    Boehringer Ingelheim (06/17/25)
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  • Sr Manufacturing Tech - 2nd Shift

    BioFire Diagnostics, LLC. (Durham, NC)
    …anticipated to be 2nd shift: Monday - Friday from 3:00pm - 11:30pm. The Sr Manufacturing Technician position is responsible for the operation of high speed equipment ... automated bottle handling, filling, vision inspection, conveying, robotic palletizing, autoclaving, labeling and / or process batching equipment in a cGMP compliant… more
    BioFire Diagnostics, LLC. (06/26/25)
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  • Senior Director - Medical Global…

    Lilly (Indianapolis, IN)
    Senior Director-Medical is delegated various responsibilities by the Associate Vice-president or equivalent role to provide leadership, supervision, coordination, ... medical and regulatory questions and requests related to products. The Sr . Director-Medical helps to ensure that the team's activities are clearly aligned with… more
    Lilly (07/08/25)
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  • Senior Director, Corporate…

    Edwards Lifesciences (Irvine, CA)
    …that we are supporting the needs and interests of the patients we serve. The Senior Director, Corporate & Regulatory Counsel role is a blend of subject matter ... legal expert and strong business acumen. The Senior Director, Corporate & Regulatory Counsel will...the Edwards Headquarters, in Irvine CA and reporting to Senior Vice President, Associate General Counsel, TAVR… more
    Edwards Lifesciences (06/12/25)
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  • Global Safety Senior Scientist

    Amgen (Washington, DC)
    …us and transform the lives of patients while transforming your career. **Global Safety Senior Scientist** **What you will do** Let's do this. Let's change the world. ... In this vital role the Global PV Sr . Scientist works with the Therapeutic Safety Teams for...Author Safety Assessment Reports and other safety documents and regulatory responses in collaboration with the GSO + Search… more
    Amgen (07/19/25)
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  • Associate Director, Oral Drug Product…

    Takeda Pharmaceuticals (Boston, MA)
    …knowledge. **Job Description** **Objective:** Under the direction of the Director or Sr . Director, ODPD, the Assoc. Director is responsible for supporting the Takeda ... drug product formulation development, process development, drug product manufacturing, regulatory support, validation thru commercialization of oral drug products… more
    Takeda Pharmaceuticals (06/26/25)
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  • Associate General Counsel, Midwest Yogurt…

    Lactalis American Group Inc. (Chicago, IL)
    …of relevant corporate and commercial transactional experience. + Experience with FDA regulatory food labeling requirements preferred. + Knowledge of promotional ... Associate General Counsel, Midwest Yogurt Division Chicago, IL...Manager of the Division, the leadership team and other senior managers of the company on all legal and… more
    Lactalis American Group Inc. (05/15/25)
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  • Wastewater Treatment Operator/ Senior

    Allegion (Indianapolis, IN)
    regulatory submittal. + Perform weekly hazardous waste inspections as per regulatory requirements. + Ensure proper labeling and management of hazardous ... individual to join our team as a Wastewater Treatment Operator or Senior Wastewater Treatment Operator, depending on experience and qualifications. This role is… more
    Allegion (06/22/25)
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  • Senior EHS Specialist

    J&J Family of Companies (Danvers, MA)
    …Plan, Flammable Storage Permit + Manage Hazardous Waste Management Plan. Ensure regulatory agency compliance ie labeling , containment, proper disposal, employee ... United States of America **Job Description:** Johnson & Johnson is currently seeking a Senior EHS Specialist to join our Abiomed team at the Danvers, MA facility.… more
    J&J Family of Companies (06/19/25)
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  • Oncology Infusion Senior Acute Pharmacy…

    Banner Health (Phoenix, AZ)
    …you are looking to leverage your abilities - apply today. As an **Oncology Senior Acute Pharmacy Technician** , you will be responsible for cleanroom procedures, IV ... better as we aim to prevent and cure cancer. As an **Oncology Infusion Senior Acute Pharmacy Technician** , you will be supported by chemotherapy trained Pharmacy… more
    Banner Health (07/21/25)
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  • Senior Supervisor of WBC Quality Assurance

    Wawa, Inc. (IA)
    …FDA and USDA labeling guidelines. + Design, execute and maintain all regulatory records and procedures to ensure all the requirements of the Appendix N program ... Duties** **:** + Manage internal and third party or regulatory audits of WD and ensures all written programs...law. If you require an accommodation, please contact our Associate Service Center at ###@wawa.com or ###. Wawa, Inc.… more
    Wawa, Inc. (06/06/25)
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  • Associate Director - Supply Chain

    Lilly (Philadelphia, PA)
    …to make life better for people around the world. **Position Overview:** The Associate Director, Supply Chain will lead and grow a supply chain team responsible ... maintaining approved suppliers/products for global operations, demand/supply/capacity planning, sourcing, labeling , dispensing, inventory management, shipping, distribution, and selection of… more
    Lilly (07/22/25)
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  • Inventory Control Associate

    ATS Automation (Souderton, PA)
    …12002 Location: Souderton, PA, US, 18964 Date: Jul 10, 2025 Inventory Control Associate Position Title: Inventory Control Associate , NCC, ATS COMPANY Automated ... expansions, and productivity improvement initiatives. Position Overview: Inventory Control Associate Support production teams by locating, staging, and issuing… more
    ATS Automation (07/10/25)
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  • Associate Director, WW Medical…

    Bristol Myers Squibb (Madison, NJ)
    …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director of WW Medical Neuroscience, Neuro degeneration Medical ... including WW Commercial, Research and Development, Global Drug Development, HEOR, Regulatory Affairs, and other global medical stakeholders. This position reports to… more
    Bristol Myers Squibb (07/22/25)
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  • Associate Director, US Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …integration points across US functional and commercialization areas to ensure alignment. The Associate Director will report to the Senior Director, US Medical ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , US Medical Neur opsychiatry position works in the US… more
    Bristol Myers Squibb (07/11/25)
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  • Research Area Specialist Inter/Assoc Lab…

    University of Michigan (Ann Arbor, MI)
    …will play a critical role in running biomarker assays using the Quanterix SR -X automated platform and the Abbott Alinity i Core Lab Instrument, developing and ... Assays & Laboratory Work: + Conduct biomarker assays using Quanterix SR -X, ensuring precision, reproducibility, and adherence to standard operating procedures… more
    University of Michigan (07/19/25)
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  • Instrument Documentation Writer - R&D Instrument…

    Grifols Shared Services North America, Inc (San Diego, CA)
    …of translations for documentation and software development. + Ensure compliance of labeling with all applicable regulatory /QSR requirements. + Create and edit ... Diego, CA. This role will be reporting to the Senior Manager, Verification and Validation. This position will provide...documentation in compliance with requirements from applicable regulatory bodies (FDA, IVDR, EUDR) and the European Union… more
    Grifols Shared Services North America, Inc (06/27/25)
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