• CT Technologist - Moncks Corner Medical Plaza…

    Roper St. Francis (Moncks Corner, SC)
    …satisfactory diagnostic images for interpretation preferred. Knowledge of OSHA, DHEC, FDA and TJC standards and regulations. Ability to operate standard office ... equipment. **Other:** Requires a mature individual who projects a professional and business-like appearance. Must maintain strict confidentiality of work-related information. **Contacts** **:** Frequent personal contact with patients, staff, physicians and… more
    Roper St. Francis (01/13/26)
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  • Clinical Research Nurse (CRN)

    Actalent (Ocala, FL)
    …enrollment, and retention. Responsibilities + Conduct clinical studies in compliance with FDA /GCP and ICH regulations and guidelines. + Provide medical care to ... patients, prioritizing their safety at all times. + Schedule subject visits within protocol windows to maximize scheduling capacity. + Perform defined study activities such as informed consent, screening, and protocol procedures including vital signs,… more
    Actalent (01/13/26)
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  • Global Work Place Principal

    The Cigna Group (Bloomfield, CT)
    …Risk Management** + Ensure all facilities comply with pharmacy regulations (DEA, FDA , Board of Pharmacy), data center standards, safety codes, and environmental ... requirements. + Execute real estate governance frameworks, ensuring data accuracy, transparency, and disciplined decision-making. + Manage risk across the portfolio, including resilience, redundancy, and operational continuity. **Financial Management** +… more
    The Cigna Group (01/13/26)
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  • Medical Laboratory Scientist - Pathology…

    Penn State Health (Lancaster, PA)
    …according to physician orders in accordance with laboratory policies and procedures, FDA , CAP, AABB, OSHA, CUA, and JCAHO regulations to facilitate optimum quality ... patient care. Tests are used in the diagnosis and treatment of disease and include specimen processing, test performance and maintaining of test results. Some procedures are complex and require professional judgment. **MINIMUM QUALIFICATION(S):** + Bachelor's… more
    Penn State Health (01/13/26)
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  • Aseptic Technician

    Actalent (Indianapolis, IN)
    …or lab experience. + Familiarity with aseptic processes in a cGMP/ FDA regulated environment. + Self-motivated and willing to accept temporary responsibilities ... outside of normal job duties. + Comfortable working in a fast-changing small company environment and able to adjust workload based on changing priorities. + Must not have unusual sensitivity to typical laboratory chemicals, including sanitization agents. +… more
    Actalent (01/13/26)
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  • Microbiology Lab Technician (Temp, 6-8 month…

    Terumo Neuro (Aliso Viejo, CA)
    …Maintain neat and legible records. + Follow cGMPs, GLPs, SOPs, USP, and FDA guidelines in all appropriate functions and notify management of any observed ... discrepancies in laboratory. + Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization. + Perform… more
    Terumo Neuro (01/13/26)
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  • Project Manager

    J&J Family of Companies (New Brunswick, NJ)
    …and PowerPoint required + Strong knowledge of manufacturing processes in FDA -regulated environments, including design, startup, and operational phases.. + Experience ... with financial management related to project or operational budgets, resource planning, and forecasting. + Familiar with Front-End Loading Best Practices. + PMP Certification Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will… more
    J&J Family of Companies (01/13/26)
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  • Director, Supplier Development Engineering

    Edwards Lifesciences (Irvine, CA)
    …project execution and compliance with internal and policies and procedures (QSR, FDA Regulations, and ISO Standards). * Partner and support product development ... efforts in the design and iteration of new delivery systems, and components for transcatheter tricuspid valve replacement technologies. **What you'll need (required):** * Bachelor's degree in a related field (Engineering, Applied Sciences, Etc.) and experience… more
    Edwards Lifesciences (01/13/26)
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  • (Manufacturing) Operations Assistant

    Colgate-Palmolive (Emporia, KS)
    …assessments as required to meet all GMP's, Food and Drug Administration ( FDA ) and AIB requirements. + Responsible to support line operations during lunches, ... breaks and coverage for open positions. + Responsible for finished goods preparation and inspection, including top cap placement, inspection checklist, legible date codes, and quality of bag seals. + Production line waste removal and disposal according to… more
    Colgate-Palmolive (01/13/26)
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  • Associate Director, Quality

    Merck (West Point, PA)
    …can interact effectively with leadership. + Strong understanding of CGMPs, FDA , and EMEA regulatory standards and strong compliance mindset; comprehension and ... use of these standards is to support the compliance and eventual sustainment of ongoing large-scaled projects, as warranted. + Demonstrated leadership and management experience working with cross-functional teams on objectives to deliver on Key Performance… more
    Merck (01/13/26)
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