• Manufacturing Sr Quality Process Expert

    L'Oreal USA (North Little Rock, AR)
    …operations in purchase and validation for new processing equipment + Ensure FDA compliance of process engineer related activities (validation of storage, validation ... of equipment, etc.) + Support quality and performance initiatives to improve metrics for the processing area + Share processing information with external groups for the development of SP's + Support investigation of non-conforming batches + Track new products… more
    L'Oreal USA (01/15/26)
    - Related Jobs

  • Sr Quality Engineer I

    Gilead Sciences, Inc. (Foster City, CA)
    …+ Ensure that changes to commercial products are conducted in accordance with FDA QSR/QMSR, ISO 13485, and other applicable standards. + Maintain compliance with ... global Risk Management processes in accordance with ISO 14791 and other applicable standards. + Work cross-functionally with Subject Matter Experts from R&D, Clinical, and Operations to ensure the risk process is applied comprehensively. + Participate in… more
    Gilead Sciences, Inc. (01/15/26)
    - Related Jobs

  • Clinical Rater

    Actalent (Gaithersburg, MD)
    …and general ethical guidelines related to clinical trials. + Become familiar with FDA regulations pertaining to clinical trials. + Review medical history with CRC ... information obtained at screening. + Reconcile medical records received for subjects and prepare PI notes to explain discrepancies, if needed. + Complete study guides and study launch with CRC. + Assist the team in managing and assessing adverse events. +… more
    Actalent (01/15/26)
    - Related Jobs

  • Research Nurse - Thoracic Head & Neck Medical…

    MD Anderson Cancer Center (Houston, TX)
    …for adverse event and safety reporting to the PI, internal/eternal IRBs and FDA . * Collection of protocol related data and documentation to be entered into ... protocol-specific databases. * Participate in all monitoring and auditing activities to maintain quality assurance. * Training and mentoring research nurses and other clinical research team members and new hires, as it relates to identifying needs, onboarding… more
    MD Anderson Cancer Center (01/15/26)
    - Related Jobs

  • Specialist SQM

    The Hershey Company (Hershey, PA)
    …time with possible weekend travel and stays required. * Thorough knowledge of FDA regulations, quality design principles, HACCP, and GMP's. * Ability to troubleshoot ... using Company-wide resources and evaluate quality systems. * Capable of understanding varied manufacturing processes to include dairy, sweeteners, confectionery, cereal, tree nuts, ground nuts, raisins, flour, baking and warehousing. * Understanding of… more
    The Hershey Company (01/15/26)
    - Related Jobs

  • Quality Assurance Scientist II

    Danaher Corporation (Chaska, MN)
    …Assurance + Experience working in a regulated industry + Knowledge of FDA regulations and ISO standards Beckman Coulter Diagnostics, a Danaher operating company, ... offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info… more
    Danaher Corporation (01/15/26)
    - Related Jobs

  • Sr. Manager - Automated Solutions

    BD (Becton, Dickinson and Company) (Sparks, MD)
    …to understand and align with applicable US Food and Drug Administration ( FDA ) regulations and Company quality system procedures, processes, policies, and tasks. + ... Proficient personal computer skills including spreadsheet skills, word processing, and other relevant applications. + Must reside within a state in the district (Kentucky, Ohio, Indiana, Illinois, Wisconsin, Michigan, Iowa, Minnesota, North/South Dakota,… more
    BD (Becton, Dickinson and Company) (01/15/26)
    - Related Jobs

  • Supervisor, Team Leader II - 3rd Shift Filling

    Bausch + Lomb (Greenville, SC)
    …in manufacturing/operations with 2+ years in supervisory role + cGMP standards and FDA (or other industry) guidelines for production + STEM degree or certification + ... Aseptic filling, Line Prep + Highly automated equipment (filling) + Continuous improvement methodologies and mindset lean, six sigma, etc. + Root cause analysis and implementing corrective actions + Ability to organize and motivate teams + Facility, Equipment,… more
    Bausch + Lomb (01/15/26)
    - Related Jobs

  • Director, US Public Affairs, HIV Communications

    Gilead Sciences, Inc. (Foster City, CA)
    …review, approval and execution of all launch communication materials in advance of FDA filing and potential approach, such as press materials, HCP and patient ... storytelling, executive training and talking points, paid partnerships. + Oversee creation, training and briefing materials for key Gilead leaders, spokespeople and third-party voices. + Advance integrated activation of paid, earned, owned and social… more
    Gilead Sciences, Inc. (01/15/26)
    - Related Jobs

  • Manager, Value Stream Cryo Operations

    Bristol Myers Squibb (Summit, NJ)
    …accountable for driving operational excellence, ensuring compliance with all regulatory requirements ( FDA , DEA, DOT, ISBT, CTPAT, OSHA, VAWD, cGMPs), and fostering a ... culture of safety, collaboration, innovation, and continuous improvement. **Shift Available:** + Wednesday - Saturday (with e/o Wednesday off), Onsite Overnight Shift, 5 pm - 5:30 am **Responsibilities:** + Lead Cryopreservation and handling of all Cell… more
    Bristol Myers Squibb (01/15/26)
    - Related Jobs