• ICSR Management Lead-Contractor - Job ID: Icsrc

    Ascendis Pharma (Palo Alto, CA)
    …our core values of Patients, Science, and Passion, we use our TransCon(R) drug development platform to fulfill our mission of developing new and potentially ... and Preventative action (CAPA) as applicable. + Supports with the oversight of regulatory and departmental compliance by ensuring timely processing of ICSRs in the… more
    Ascendis Pharma (08/09/25)
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  • Project Manager I

    Charles River Laboratories (Northridge, CA)
    …multiple high-impact projects simultaneously. Experience in client communication, regulatory environments, and process improvement is highly desirable. Essential ... across internal workflows. + Collaborate with departments such as R&D, Quality, Regulatory , and Manufacturing to meet project goals. + Ensure projects adhere to… more
    Charles River Laboratories (08/08/25)
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  • Endoscopic Repair Technician

    Fujifilm (Wayne, NJ)
    …Meet and/or exceed deadlines. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 ... standard requirements and all other applicable laws, regulations, and standards. + Other related duties as required. **Qualifications:** + HS Diploma or equivalency is required. + Electronic and/or Mechanical Certification or degree preferred. + Minimum 2… more
    Fujifilm (08/08/25)
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  • Sales Specialist, Diagnostic Oncology (West Coast)

    Fujifilm (San Juan, PR)
    …other duties as assigned. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 ... standard requirements and all other applicable laws, regulations, and standards. + Comply with and pass all requirements for vendor credentialing as part of gaining access to hospitals and facilities to perform assigned job duties. **Qualifications** + BA/BS… more
    Fujifilm (08/03/25)
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  • Clinical Training Director

    ConsignMed (New Orleans, LA)
    …industry credentialing requirements/standards. Clear and complete background investigation and drug screen, complete immunizations and pass regulatory exams. ... Benefits: * Competitive salary and benefits package. * Opportunity to make a significant impact on patient care through effective training. * Career growth potential more
    ConsignMed (07/18/25)
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  • Open Rank Pediatric Sedation Physician

    University of North Carolina- Chapel Hill (Chapel Hill, NC)
    …translational researchers at all levels. This support includes seed funding, regulatory assistance, data management, drug /device development and grant ... preparation among other things. The North Carolina Children's Hospital is part of a busy quaternary care medical center with a 20 bed multidisciplinary PICU / PCICU that admits over 1200 patients per year and supports an active pediatric cardiothoracic surgery… more
    University of North Carolina- Chapel Hill (07/08/25)
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  • Specialist, Clinical Apps - MRI

    Fujifilm (Raleigh, NC)
    …and system enhancement suggestions. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO ... 13485 standard requirements and all other applicable laws, regulations, and standards. **Qualifications** + Experience + Minimum three (3) years clinical MR experience. + Educational requirements: + Degree from accredited Radiology Technologist Program. +… more
    Fujifilm (07/02/25)
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  • Pharmacist(Clinical Spec)

    Veterans Affairs, Veterans Health Administration (Kansas City, MO)
    …the patient's medication therapy. Effectively monitors and assesses patient outcomes to drug therapy, managing ongoing therapy or transition to other levels of ... treatment. Monitors for and reports drug errors, adverse drug reactions, allergies and...each step in the dispensing process according to law, regulatory standards, VHA policies and standard of care to… more
    Veterans Affairs, Veterans Health Administration (09/16/25)
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  • Process Development Senior Scientist - Analytical…

    Amgen (Thousand Oaks, CA)
    …method transfer, process and product development support, and GMP testing of late phase drug substances and drug products. The Scientist will work closely with a ... for synthetic molecules release testing and characterization + Collaborate closely with drug substance and drug product process development colleagues to achieve… more
    Amgen (09/14/25)
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  • Finance & Accounting Director III-SES, Pending…

    MyFlorida (Orlando, FL)
    …travel; feel collections; third party billing, in accordance with appropriate regulatory procedures. Oversee accounts payable including the preparation of the ... Oversee the agency's purchasing functions and ensure compliance with appropriate regulatory policies relative to same, including approving purchase orders and… more
    MyFlorida (09/11/25)
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