• Associate Machinist

    Integer Holdings Corporation (Salem, VA)
    …Environmental and Security Management Systems, US Food and Drug Administration ( FDA ) regulations, company policies and operating procedures, and other regulatory ... requirements * Operates and sets up CNC equipment with assistance * Accountable for meeting cycle time and yield expectations. * Sharpens tooling as needed to maintain tolerances * Makes adjustments and monitors assigned equipment to ensure dimensional part… more
    Integer Holdings Corporation (01/11/26)
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  • Patient Access Liaison - UPLIZNA - Southwest

    Amgen (Denver, CO)
    …+ Orphan or Rare disease experience. + Familiarity with HIPAA guidelines and FDA requirements. + Familiarity with and Adherence to internal and OIG Compliance ... guidelines a must + Ability to handle difficult patient cases and resolve hurdles. + Ability to work in team environment and manage communication with case Liaisons and sales reps. + Ability to respond immediately when necessary (within 24 hours) to prevent… more
    Amgen (01/11/26)
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  • Technician II, Manufacturing - 1st shift

    Abbott (Plymouth, MN)
    …requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes, ... and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. **Required Qualifications** + High school diploma or trade school certification, specialized… more
    Abbott (01/11/26)
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  • Biomedical Equipment Support Specialist…

    Veterans Affairs, Veterans Health Administration (Portland, OR)
    …medical devices and clinical systems such as Food and Drug Administration ( FDA ), Federal Information Security Modernization Act (FISMA), and National Institute of ... Standards and Technology (NIST) guidelines. (f) Ability to apply information security tools including virus protection, software updates, and operating system patches. (g) Ability to establish a medical network including VLAN configuration, Internet Protocol… more
    Veterans Affairs, Veterans Health Administration (01/11/26)
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  • Sr Engineer II - Electrical

    Takeda Pharmaceuticals (Social Circle, GA)
    …executing engineering projects, and supporting facility issues, in a FDA -regulated manufacturing environment. + Excellent technical problem-solving skills are a ... must. + Must have excellent organizational, verbal and written communication skills; able to efficiently communicate with cross-functional teams and management on recommended course of action, with minimal assistance. + Apply Lean Manufacturing principles and… more
    Takeda Pharmaceuticals (01/11/26)
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  • QA Associate II

    BD (Becton, Dickinson and Company) (Mebane, NC)
    …+ Basic knowledge of SAP is preferred. + Experience working in an FDA regulated environment is highly desirable. **Knowledge and Skills:** + General Proficiency in ... Microsoft Office + Demonstrated understanding of sampling techniques and inspection standards. + Basic math skills and the ability to utilize Excel for basic calculations and graphing. + Must be able to speak, read, and write English fluently as well as write… more
    BD (Becton, Dickinson and Company) (01/11/26)
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  • Executive Director, Human Research Protection…

    University of Maryland, Baltimore (Baltimore, MD)
    …Abilities _* Knowledgeable in the provision of the Common Rule (45CFR46), FDA regulations, ICH Good Clinical Practice Guidelines, and other relevant requirements and ... guidelines related to the ethical study of human research subjects. Thorough knowledge of position requirements. Thorough knowledge of all applicable requirements, regulations, and laws. Skill in effective use of applicable technology/systems. Ability to… more
    University of Maryland, Baltimore (01/11/26)
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  • Sr. Human Factors Engineer

    Actalent (Providence, RI)
    …regulatory standards. + Ensure compliance with regulatory and industry standards such as FDA Human Factors Guidance and ISO 9241. + Develop and conduct human factors ... research studies independently or with clients and/or government agencies. + Plan and conduct user evaluations of product concepts, analyze data, and document evaluation methods/results in detailed reports. Present design recommendations to the project team. +… more
    Actalent (01/11/26)
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  • Packaging Machine Operator - 12-Hour Night Shift

    Abbott (Columbus, OH)
    …dates. + This position is accountable for complying with applicable FDA , GMP, OSHA and Abbott/Ross regulations, policies, procedures or guidelines. **SHIFT ... + PAY** Pay: $20.05/hour plus 5% shift premium Rotating 12-hour night shift - 6:00pm to 6:30am Example of rotating schedule: + Week 1: Sun, Wed, Thurs + Week 2: Mon, Tues, Fri, Sat **MINIMUM QUALIFICATIONS** + High school diploma or GED + Prior manufacturing,… more
    Abbott (01/11/26)
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  • QA Inspector- (Multiple Openings)

    Astrix Technology (Chino, CA)
    …personal care products comply with industry regulations and standards, such as FDA guidelines, and work towards continuous improvement in meeting these requirements. ... + Collaborate with production and quality teams to identify areas for process improvement and implement corrective actions to prevent defects and non-conformities. + Communicate with the production team to address and resolve quality issues, deviations, or… more
    Astrix Technology (01/11/26)
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