• Quality Manager

    Nissha Medical Technologies (Colorado Springs, CO)
    …establish clear goals, and support learning opportunities for job skills and career growth. Quality Control and Quality Assurance: + Implement and ensure ... Quality Manager Summary **Title:** Quality Manager...ISO 13485 standards and is conducted in accordance with cGMP regulations in all areas. + Oversee the resolution… more
    Nissha Medical Technologies (09/19/25)
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  • Senior Manager, CTO Network QA Disposition

    Bristol Myers Squibb (Summit, NJ)
    …+ Approve change controls related to disposition and associated activities including Quality Control specifications. + Performs projects as required by senior ... **Knowledge & Skills:** + Must have advanced knowledge and experience with cGMP manufacturing, Quality , and compliance. + Demonstrated ability to work… more
    Bristol Myers Squibb (10/16/25)
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  • Materials Handler I

    PCI Pharma Services (Bedford, NH)
    …with all aspects of logistics such as receiving, shipping, data entry, inventory control , labeling and maintaining all associated cGMP documentation as needed. ... Handler I assists in the day-to-day activities relating to inventory control functions supporting pharmaceutical fill/finish operations. The main responsibility of… more
    PCI Pharma Services (10/11/25)
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  • Quality Systems Manager for Plasma Center

    Grifols Shared Services North America, Inc (Lincoln, NE)
    …and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. + Collaborates ... over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company...Ensures that job and center annual training (ie Advanced cGMP , Blood Borne Pathogen, and others as may be… more
    Grifols Shared Services North America, Inc (10/17/25)
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  • Quality Specialist

    Actalent (Princeton, NJ)
    …(Ishikawa), and FMEA to support investigations. + Collaborate cross-functionally with Manufacturing, Quality Control , and Supply Chain teams to resolve ... Job Title: Quality Specialist Job Description We are seeking a...operations, including in-process checks, deviation identification, and adherence to cGMP expectations. + Ensure all manufacturing activities comply with… more
    Actalent (10/17/25)
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  • Senior Specialist, Quality Assurance

    Cardinal Health (Helena, MT)
    …job family provides oversight of production/manufacturing activities, training to operational and quality control personnel, and educates business leaders on ... or equivalent work experience, preferred + Working knowledge of cGMP and FDA regulations. + Experience with quality... cGMP and FDA regulations. + Experience with quality management systems and labeling platforms (eg, Veeva, Kallik,… more
    Cardinal Health (10/15/25)
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  • Quality Systems Manager

    Biomat USA, Inc. (Charlotte, NC)
    …federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. . Maintains ... and services in more than 110 countries and regions. ** Quality Systems Manager (QSM)** **PRIMARY RESPONSIBILITIES** : . Evaluates...Ensures that job and center annual training (ie Advanced cGMP , Blood Borne Pathogen, and others as required) is… more
    Biomat USA, Inc. (10/13/25)
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  • Quality Auditor, Second Shift

    Henkel (Geneva, NY)
    …and make an impact at Henkel. **What you'll do** + Perform regular quality control inspections, including but not limited to quantitative dimensional testing ... acceptance decision based on test results. + Perform regular quality control inspections throughout the production run...+ Must demonstrate good teamwork ability. + Knowledge of cGMP requirements is a plus + Strong attention to… more
    Henkel (09/18/25)
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  • Senior Chemist

    ADM (Kennesaw, GA)
    …the following: **Testing and Reporting** + Test submitted samples under cGMP /GLP environment as per company's standard operating procedures and USP/FDA guidelines. ... Review and approve the interpretation and documentation of results generated by QC Chemists + Ensure analytical results are appropriately documented and reported in… more
    ADM (09/17/25)
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  • Manufacturing Associate I - Night Shift

    Takeda Pharmaceuticals (Brooklyn Park, MN)
    …and document daily manufacturing operations according to SOPs in a cGMP environment. You will operate biologics production equipment (bioreactors, filtration units, ... systems and fixed/portable vessels. + Perform basic trouble shooting. + Document cGMP data for processing steps and equipment activities while following standard… more
    Takeda Pharmaceuticals (10/07/25)
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