• Sr. MES Opcenter OR Camstar Consultant - Remote

    Cognizant (Trenton, NJ)
    …teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the paper Batch record and ... the shopfloor transaction using OpCenter Execution Discrete in Discrete manufacturing Industry Experienced in Camstar (V8.x) Modeling Configuration, Designer,… more
    Cognizant (07/18/25)
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  • Quality Compliance Auditor

    embecta (Parsippany, NJ)
    …in quality compliance or a related role within the Medical Device or Pharmaceutical manufacturing industry. + In-depth knowledge of FDA regulations, ISO 13485, ... is a critical role within embecta, a global leader in medical device manufacturing . This position ensures that all quality systems and operations comply with… more
    embecta (08/08/25)
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  • Sr. Design Quality Engineer I

    Integra LifeSciences (Princeton, NJ)
    …5+ years of experience in Quality Assurance role for medical device or pharmaceutical manufacturing , or equivalent education and years of experience. Or, ... + Experience using eQMS software solutions. + Knowledge of current Good Manufacturing Practices (cGMP) and other applicable standards. + Experience using analytical… more
    Integra LifeSciences (06/11/25)
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  • Lead Engineer, CSV

    Bristol Myers Squibb (Summit, NJ)
    …to identify and document User and Functional Requirements. + Knowledge of pharmaceutical laboratory and manufacturing systems. + Experience executing equipment ... System Validation (CSV) Engineer** supports the successful implementation of manufacturing and laboratory equipment and computerized systems at multi-use sites… more
    Bristol Myers Squibb (08/30/25)
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  • Quality Assurance Engineer II

    Integra LifeSciences (Plainsboro, NJ)
    …of experience in a Quality Assurance role for medical device or pharmaceutical manufacturing . + Demonstrates knowledge of investigations, root cause analysis, ... quality systems, the CAPA system and technical writing. + Demonstrates excellent organizational and communication skills. + Proficient with the MS Office Suite, and statistical software. + Must be able to work independently with minimal supervision. Integra… more
    Integra LifeSciences (08/17/25)
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  • IT-Systems Administrator

    Xybion Corporation (Princeton, NJ)
    …we digitize drug research and development, laboratory testing, regulatory approvals, and pharmaceutical manufacturing on a single, unified cloud platform that is ... cost-effective, ready to deploy, and easy to use. Highly regulated companies choose Xybion to help them become more efficient, reduce costs and manage compliance, regulatory adherence and risk. Since our founding in 1977, we have supported through software,… more
    Xybion Corporation (07/11/25)
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  • Senior Account Manager

    Hovione (East Windsor, NJ)
    …top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and ... related commercial area in the pharmaceutical sector * Experience of pharmaceutical product development and manufacturing (preferred) * Experience in leading… more
    Hovione (08/08/25)
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  • Laboratory Instrumentation Supervisor

    CBRE (Princeton, NJ)
    …The services will be delivered in a Quality Control Laboratory to a Pharmaceutical client manufacturing product. **What you'll do** + Supervises, plans, directs, ... genomics, as well as contract research organizations (CROs) and contract manufacturing organizations (CMOs). Our comprehensive range of services includes laboratory… more
    CBRE (08/29/25)
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  • MIQA Reliability Engineer

    DuPont (Parlin, NJ)
    …industry) with a focus on MIQA, reliability, or PSM, preferably in a pharmaceutical or food manufacturing environment . Strong analytical skills with ... demonstrated ability to consistently solve problems in a decisive and efficient manner . Understands MIQA policy requirements for Process Safety Management (S21A), statutory & regulatory requirements as applicable, and Recognized And Generally Accepted Good… more
    DuPont (06/23/25)
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  • Compliance Investigator

    Actalent (Allendale, NJ)
    …writing and reviewing deviations and investigations. + Experience working within a pharmaceutical company supporting manufacturing . + Experience within a quality ... + Write and complete investigations and deviations to ensure compliance with manufacturing and GMP standards. + Conduct root cause analysis and manage the… more
    Actalent (08/28/25)
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