• Occupational Therapist

    Banner Health (Torrington, WY)
    …accordance with physician referral, state and local organizational standards, regulatory agencies, and established departmental policies and procedures. This ... 3. Documents according to standards set by the department and regulatory agencies. Documents legibly. Completes documentation within the established time frames… more
    Banner Health (07/23/25)
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  • Director of Quality Management - Inpatient Rehab

    Select Medical (Cleveland, OH)
    …Improvement and Patient Safety programs in accordance with the guidelines and regulatory requirements of Federal and State regulations on a hospital-wide basis. ... Develops and Reviews policies and procedures to ensure compliance with all regulatory and accrediting standards. Collects data to monitor compliance and/or trends. +… more
    Select Medical (07/23/25)
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  • Senior Client Relationship Specialist

    Mizuho Corporate Bank (Los Angeles, CA)
    …helping to build a collaborative work environment. A strong understanding of regulatory requirements and strict adherence to internal policies and procedures are ... financial services + Strong knowledge of banking products, services and regulatory requirements + Bilingual English/Japanese and multilingual ability may be… more
    Mizuho Corporate Bank (07/23/25)
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  • Medical Writing Clinical Publisher

    Teva Pharmaceuticals (West Chester, PA)
    …to make a difference with. **The opportunity** A Clinical Publisher in Global Regulatory Medical Writing (GRMW) Operations provides basic support to GRMW (and other ... production of submission-ready clinical research documentation in support of drug development, product registrations, and product marketing. The Clinical Publisher's… more
    Teva Pharmaceuticals (07/22/25)
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  • Gen AI POD Captain

    Astellas Pharma (Northbrook, IL)
    drug discovery and development process, clinical trials, and regulatory submissions. + Bioinformatics and Computational Biology: + Knowledge of bioinformatics ... platform development and deployment **Pharmaceutical Industry Knowledge:** + GxP and Regulatory Compliance: + Familiarity with Good Practices (GxPs), regulatory more
    Astellas Pharma (07/22/25)
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  • QA Supervisor, Batch Release

    ThermoFisher Scientific (Greenville, NC)
    …Practices (GMP) Safety Standards, Office **Job Description** **GROUP/DIVISION SUMMARY** The Drug Product Division - North America (DPD-NA) is one of the ... sites who specialize in taking sterile injectable and oral solid dose drug products from development to commercialization. **POSITION SUMMARY** The Quality Assurance… more
    ThermoFisher Scientific (07/20/25)
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  • Physical Therapist Assistant

    Banner Health (Phoenix, AZ)
    …accordance with physician referral, state and local organizational standards, regulatory agencies, and established departmental policies and procedures. This ... Therapist. 3. Documents according to standards set by the department and regulatory agencies. Completes documentation within the established time frames of the… more
    Banner Health (07/19/25)
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  • Sr Associate, Technical Sales- Integrated Systems

    West Pharmaceutical Services (Exton, PA)
    …uncovering opportunities through strong listening and interviewing skills, understanding their drug pipeline, and offering tailored solutions that align with their ... serviced. + Understand market trends including relevant competitors, technology and regulatory issues to keep customer informed + Utilize all service platforms,… more
    West Pharmaceutical Services (07/19/25)
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  • Hospice Medical Director

    CareOregon (Portland, OR)
    …satisfactory completion of a pre-employment background check, immunization review, and drug screen (including THC/Marijuana). CareOregon is a federal contractor and ... to improve care delivery, use resources effectively, and comply with legal, regulatory and clinical policies and procedures. This position is an integral part… more
    CareOregon (07/19/25)
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  • Director, Biologics Analytical Development…

    Gilead Sciences, Inc. (Foster City, CA)
    … substance and drug product. + Proven track record in drafting regulatory documentation at all stages, including **IND, BLA, and PAS** filings. + Demonstrated ... deliverables. + Serve as an author and reviewer of CMC sections in regulatory filings, and support interactions with health agencies. + Collaborate across Gilead… more
    Gilead Sciences, Inc. (07/18/25)
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