• Surmasis Pharmaceutical - Director of Quality…

    Katecho (Des Moines, IA)
    …all products manufactured by the organization meet customer specifications and regulatory requirements and achieve superior quality and reliability levels. This ... operations of the Quality Department functions of Surmasis as a Pharmaceutical Drug contract manufacturer. Products within the scope of the company include, but… more
    Katecho (08/08/25)
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  • Sous Chef

    Sunrise Senior Living (Bethesda, MD)
    …quality service standards and complies with all federal, state, local regulatory procedures regarding food production and food presentation. **RESPONSIBILITIES & ... complete and filed per Sunrise quality service standards and regulatory compliance. + Reviews to ensure all side-work and...with Sunrise is conditioned on completing and passing a drug test (which does not include marijuana), participating in… more
    Sunrise Senior Living (08/08/25)
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  • Production Planning D / Explosives Control…

    L3Harris (Cincinnati, OH)
    …Bureau of Alcohol, Tobacco Firearms, and Explosives (BATFE), and other regulatory requirements. + Oversee the receipt, storage, handling, transportation, and ... disposal of explosive materials in accordance with company procedures and regulatory requirements. + Conduct regular inspections and audits of explosive materials… more
    L3Harris (08/08/25)
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  • Reliability Reporting Manager

    Pacificorp (Salt Lake City, UT)
    …+ Represent the company when interfacing with commercial counterparties, state regulatory commissions, and other state regulatory stakeholder groups. + ... + A minimum of seven years of experience in regulatory compliance and data analysis, or a related area....upon the successful completion of a background check and drug screening including for marijuana. While marijuana is legal… more
    Pacificorp (08/07/25)
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  • Clinical Research Coordinator

    University of Utah (Salt Lake City, UT)
    …operations. This role is critical in ensuring that study documentation, regulatory processes, and trial management practices align with institutional, sponsor, and ... research study teams, and clinical teams, the QA Specialist ensures regulatory compliance, operational efficiency, and consistently high standards of documentation… more
    University of Utah (08/07/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and ... assessments including collection of blood samples, processing and shipment. Maintain drug accountability, adequate study supplies and equipment. The coordinator will… more
    Stanford University (08/07/25)
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  • Data Coordinating Center Project Manager II

    University of Utah (Salt Lake City, UT)
    …multi-site research. Bring your background in strong clinical research, protocol development, regulatory and single IRB experience to the Utah DCC . Autonomy, ... Functions:** 1. Independently provides oversight for all aspects of study conduct, regulatory compliance, and record keeping processes at the site or institution… more
    University of Utah (08/07/25)
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  • Program Supervisor

    YAI (Milford, NY)
    …Ensures program quality and compliance with Federal, State, local and other regulatory requirements, oversees clinical programming, serves as an advocate for the ... practices and in line with Federal, State, Local and regulatory requirements. + Provides effective leadership and develops a...no more than 5 points + New Jersey State drug test screening is mandatory prior to employment and… more
    YAI (08/03/25)
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  • Wealth Regional Supervisor

    Truist (Richmond, VA)
    …job description:** Purpose: Mitigate risk for the firm from financial, reputation and regulatory items by ensuring that the advisors, OSJs and/or branch offices are ... suitability and required documentation has been met. Focus on meeting all regulatory requirements pertaining to transaction review. Perform a holistic view of… more
    Truist (08/02/25)
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  • Manager, PVRM

    Sumitomo Pharma (Madison, WI)
    …but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and Biostatistics is essential. **Job Duties ... as required. + Coordinate responses to ad hoc safety issues such as regulatory authority, site, or health care professional requests, along with PV physician,… more
    Sumitomo Pharma (08/01/25)
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