• Quality Specialist - AVS

    Merck (West Point, PA)
    …Review, Documentations, Environmental Monitoring, Environmental Monitoring Systems, FDA Regulations, GMP Compliance, Immunochemistry, Interpersonal Relationships, IS ... Audit, Laboratory Operations, Laboratory Quality Control, Management Process, Problem Solving Therapy, Quality Inspections, Quality Operations {+ 5 more} **Preferred Skills:** Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)… more
    Merck (01/13/26)
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  • Senior Engineer Enabling Analytics & System…

    J&J Family of Companies (Horsham, PA)
    …Knowledge of the drug development process, including Good Clinical Practices (GCPs) and FDA Code of Federal Regulations + The ability to partner with stakeholders ... and influence decision-making across a matrix organization + Excellent analytical, problem solving, communication and presentation skills + Global business mindset + Ability to travel up to 10% of the time (Domestic/International) **Preferred:** + Experience… more
    J&J Family of Companies (01/13/26)
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  • CD&D Beverage Scientist Alcohol

    ADM (Erlanger, KY)
    …including pasteurization, homogenization, carbonation, and aseptic techniques. + Familiarity with FDA food labeling regulations and nutritional claims, as well as ... TTB regulations related to alcoholic beverages. + Excellent project management and problem-solving skills; able to prioritize and drive multiple initiatives forward. + Competency in data analysis, experimental design, and technical reporting. + Strong… more
    ADM (01/13/26)
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  • Health, Safety, and Environmental Associate

    Lilly (Concord, NC)
    …for training and benchmarking with other Lilly sites. + cGMP standards and FDA (or other industry) guidelines for production + HSE incident investigation, including ... multiple root cause analysis methods. + Facilitating employee safety teams, with the goal of turning over leadership to operations employees. + Managing a contractor safety program across a large footprint. + Implementation of electronic permit to work systems… more
    Lilly (01/13/26)
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  • Project Manager

    Abbott (Westfield, IN)
    …levels of management + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies and Business Units operating ... procedures **Required Qualifications** + Bachelor's degree in engineering or related field + Eight (8) years of medical device experience in R&D, Manufacturing and/or Quality Engineering + Excellent verbal and written communication skills, with the ability to… more
    Abbott (01/13/26)
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  • Clinical Sciences Professional (Intermediate)

    University of Colorado (Aurora, CO)
    …+ Adhere to institutional, regulatory, and ethical guidelines, including HIPAA, CAP/CLIA, FDA , and NIH best practices. + Assist in developing and revising standard ... operating procedures (SOPs). **Collaboration & Administrative Support (10%)** + Serve as a liaison between clinical care teams, pathology personnel, and researchers. + Coordinate fulfillment of specimen requests and prepare shipments for approved… more
    University of Colorado (01/13/26)
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  • Supervisor, Quality Control

    AbbVie (Worcester, MA)
    …defend, persuade Corporate/Plant practices with outside organizations. Routinely meet with regulators ( FDA & EU) and customers to ensure no interruption in business ... due to compliance issues. + Directs area of responsibility to meet production objectives within planned budgets. Provides input to Supervisor for resources needed to construct budget, updates, and changes in financial plan. Supervises area supplies and… more
    AbbVie (01/13/26)
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  • Scientist 2, QC Analytical Development Chemistry

    Fujifilm (Holly Springs, NC)
    …* Ensures compendial method oversight and scientific guidelines (eg ICH, EMA, FDA , etc.) * Supports regulatory requests and inspections * Supports the QC ... AD team to investigate any project challenges with necessary risk assessment tools and techniques * Supports best practices for TT and PPQ strategies globally, as required * Performs other duties, as assigned **Minimum Requirements:** * BS in Chemistry,… more
    Fujifilm (01/13/26)
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  • Microbiology Analyst

    Actalent (Hercules, CA)
    …with relevant experience in microbiology. + 2+ years of GMP/GLP laboratory/ FDA experience. Additional Skills & Qualifications + BS/BA in Biology, Pharmaceutical ... Sciences, Biotechnology, or equivalent, with a preference for a Microbiology degree. + 2+ years of relevant microbiology experience or an Associate degree with 5+ years of experience in a related field, or a High school diploma with 7+ years of experience. +… more
    Actalent (01/13/26)
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  • Senior Director, Process Engineering & Maintenance

    Fujifilm (Holly Springs, NC)
    …project-driven organization + Experience in a CGMP facility or working with FDA regulations Preferred Qualifications: + Prior experience in a similar role in ... large projects from conceptual design phase to operations + 4+ years of experience leading and developing leaders + Experience leading manufacturing or technical departments Physical Requirements: + May work in Mechanical/Production spaces that may require… more
    Fujifilm (01/13/26)
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