• AD Market Research/Competitive Intelligence - CRM

    Boehringer Ingelheim (Ridgefield, CT)
    …BI personnel in other countries Ensures that corporate standards of excellence and compliance are upheld and performs all Company business in accordance with all ... regulations (eg EEO, FDA , OSHA, PDMA, EPA, PhRMA, SCIP etc.) and Company...Continuous Improvement: Share knowledge of research methodologies and high quality vendors with other managers in the department. Improve… more
    Boehringer Ingelheim (08/19/25)
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  • Customer Fulfilment Manager

    Sanofi Group (Morristown, NJ)
    …packaging, labeling and distribution activities and partnership initiatives + ** Compliance Oversight:** Ensure all outsourced activities and partnerships comply with ... FDA regulations, cGMP requirements, and internal procedures **About You**...a wide range of health and wellbeing benefits including high- quality healthcare, prevention and wellness programs and at least… more
    Sanofi Group (08/17/25)
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  • Patient Delivery Rep, Rx Partners (Casual)

    UPMC (Bridgeville, PA)
    …in timely, safe and accountable manner. + Promote UPMC culture by providing quality , comprehensive services to all customers through a team approach. + Complete ... and/or equipment according to policy. + Maintain accurate and complete records in compliance with State, local, and Federal laws and/or regulations (including FDA more
    UPMC (08/16/25)
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  • Corporate Wellness Manager (Dietitian)

    Compass Group, North America (San Francisco, CA)
    …policies to implement wellness related programs and initiatives and to ensure compliance with FDA nutrition labeling laws. **Key Responsibilities:** + ... Manager I.** The **Wellness Manager** implements corporate nutrition programs, supporting quality assurance in areas of nutrition labeling, food allergies and… more
    Compass Group, North America (08/15/25)
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  • Principal Engineer, Idap TS/MS Product (R3 - R5)

    Lilly (Indianapolis, IN)
    …1 year of experience with design and execution of experimental trials in compliance with SOPs, FDA /ICH guidelines, DEA regulations, and safety requirements for ... site. Provide technical support on non-routine investigations, including on quality and stability. Prepare technical documents including annual product reviews,… more
    Lilly (08/15/25)
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  • Clinical Research Nurse C/D (Abramson Cancer…

    University of Pennsylvania (Philadelphia, PA)
    …trials. Participate in the conduct of audits by study sponsors, CROs, the FDA , the Eastern Oncology Group, the University of Pennsylvania's CTSRMC, and other groups. ... Participate in core study team, disease-site group and ongoing protocol training/ compliance meetings. Participate in working groups within the disease-site team that… more
    University of Pennsylvania (08/15/25)
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  • Executive Director, Clinical Development - Rare…

    Amgen (Thousand Oaks, CA)
    …diligence and business development activities as needed + Always operate within Compliance Guidelines + Provide medical monitoring oversight for clinical trials as ... toxicology approaches + Knowledge of Good Clinical Practices (GCP), FDA regulations and guidelines, and applicable international regulatory requirements +… more
    Amgen (08/14/25)
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  • Clinical Research Coordinator - Department…

    Wayne State University (Detroit, MI)
    …where students from all backgrounds are offered a rich, high- quality education. Our deep-rooted commitment to excellence, collaboration, integrity, diversity ... completed accurately, in a timely manner per sponsor requirements. Ensure compliance with protocol guidelines and regulatory agency requirements. Collect, process,… more
    Wayne State University (08/14/25)
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  • Medical Screener - Start Your Career in Healthcare…

    Kedplasma (Williamsville, NY)
    …donation, nutrition, and safety best practices + Assisting with audits and ensuring compliance with FDA , EU, and company guidelines **Why This Role Matters:** ... hands-on training with room to grow into other roles (like Phlebotomist or Quality Tech) + Full-time schedule with consistent hours + Competitive pay, health… more
    Kedplasma (08/14/25)
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  • Associate Project Engineer - Sustaining

    Globus Medical, Inc. (Audubon, PA)
    …we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the ... Reports (PMSR)** and **Periodic Safety Update Reports (PSUR)** in compliance with global regulatory standards. + Drive **risk analyses**...or complaint handling systems. + Understanding of ISO 13485, FDA 21 CFR Part 820, or EU MDR regulations.… more
    Globus Medical, Inc. (08/14/25)
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