• Director, Medical Information & Review

    Takeda Pharmaceuticals (Lexington, MA)
    …responses, including clinical dossiers. + Responsible for ensuring team provides high- quality , balanced and timely medical information for multiple products upon the ... alignment with USM Medical Strategies, and support the delivery of high- quality product information, promotional product communications, and other medical and… more
    Takeda Pharmaceuticals (08/15/25)
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  • Distribution Coordinator

    Catalent Pharma Solutions (Kansas City, MO)
    …to 3:30pm.** **Catalent is committed to a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer, and ... The Distribution Coordinator will ensure work is carried out in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating… more
    Catalent Pharma Solutions (08/15/25)
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  • Physician - Chief of Pathology and Laboratory…

    Veterans Affairs, Veterans Health Administration (Erie, PA)
    …CFR | 17.35000. Working with the Executive Director, PLM and the National PLM Quality and Compliance Officer to ensure that corrective action is implemented ... and ensuring that laboratory testing is carried out in compliance with 42 CFR part 493 as applied in...functions of the VA medical facility PLM. Ensuring that quality patient services are provided to VA patients and… more
    Veterans Affairs, Veterans Health Administration (08/14/25)
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  • Production Lead

    Kedplasma (Pensacola, FL)
    …maximize donor retention. + Identifies all potential, serious or chronic problems affecting quality of compliance . + Performs opening and closing duties in ... feel objects, tools or controls. Duties and Responsibilities: + Ensures the compliance of all Center activities with DCOP's (Donor Center Operating Procedures) and… more
    Kedplasma (08/14/25)
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  • Cardiac Research Coordinator

    HCA Healthcare (Overland Park, KS)
    …responsibilities. + Coordinates and manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical Practices and IRB requirements. ... are performed by approved research staff and ensure protocol compliance . + Maintain professional relationships with sponsors, Clinical Research Organizations,… more
    HCA Healthcare (08/10/25)
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  • Business Analyst - Supply Chain Kinaxis Maestro

    Lilly (Indianapolis, IN)
    …and Agile experience. + Understanding of pharmaceutical manufacturing processes and compliance with industry-specific regulations, such as FDA guidelines for ... You will be part of Tech at Lilly MQ (Manufacturing and Quality ) an organization that drives manufacturing operational excellence through utilization of technology.… more
    Lilly (08/08/25)
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  • Senior Commissioning/Validation Specialist

    Stantec (New York, NY)
    …us create buildings that matter to our world. Together, we are enhancing the quality of life globally through design. Join us and design your place with Stantec. ... related to bio-pharmaceutical dosage forms, nutraceutical facilities and other regulated FDA or similar facilities where drug products are manufactured, stored in… more
    Stantec (08/07/25)
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  • Mammography Tech 1

    University of Rochester (Rochester, NY)
    …+ Assists leadership with all QA and QC tests and documentation to ensure compliance with MQSA and FDA standards. Other duties as assigned. **MINIMUM EDUCATION ... exams by following and verifying referring providers' orders and remaining in compliance with the Imaging Sciences department and all governing bodies. Responsible… more
    University of Rochester (08/07/25)
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  • Regulatory Affairs Manager - Vascular (on-site)

    Abbott (Santa Clara, CA)
    …development and manufacturing teams + Prepare robust regulatory applications ( FDA and international regulatory agencies) to achieve departmental and organizational ... regulatory and related teams + Assess the acceptability of development, quality , preclinical and clinical documentation for submission filing. Compile, prepare,… more
    Abbott (07/31/25)
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  • Automation Controls Lead

    Envista Holdings Corporation (Pomona, CA)
    …internal procedures. + Initiate equipment modifications to improve productivity and product quality . + Work with outside vendors to coordinate the development of ... and budget forecasts. + Must demonstrate responsibility for the quality and financial aspects of the company. + Pursue...manufacturing environment. + Familiarity with health and safety regulations ( FDA Regulations & ISO 13485 Knowledge) is plus +… more
    Envista Holdings Corporation (07/31/25)
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