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    ME

    Medvacon

    Life Sciences

    GMP Quality Validation - Lab

    Kansas City, United StatesOn-SiteContract3+ yrs experiencePosted 3w ago
    All Medvacon jobs

    Job description

    Validation representative for laboratory validation activities, including Equipment Qualification and systems administration. In addition, provide technical guidance as a SME with respect to validation/process deviations and change controls as pertains to validation impact.

    This is on W2 only

    No expenses

    ONSITE

    SHIFT - M-F 8-4PM -DURATION

    1 YEAR WITH OPTION TO EXTEND

    Bachelors in related Field or 2-10 years of Scientific or Engineering experience

    3+ years work exp in project/process engineering and validation of FDA-covered processes, as well as QA experience in a pharmaceutical environment.

    Please attach a WORD resume to your submission

    All of your information will be kept confidential according to EEO guidelines.

    ON-SITE only

    This is a contract role and does not offer benfits

    40-hour week

    1 YEAR WITH OPTION TO EXTEND -

    Job details are sourced from the employer's original posting.

    Open job posting
    ME

    About the company

    Medvacon

    MEDVACON Life Sciences works with many leading pharmaceutical companies to hire temporary and full-time employees to join their organization. We're providing hiring support for our pharma client located in Foster City, CA for 2 Research Assocaites in the Foster City location.

    View all Medvacon jobs
    Industry
    Life Sciences
    Open roles
    7

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