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    Validation - Specialist, MSEO Manufacturing Systems Validation - Summit, United States - Sunrise Systems

    Sunrise Systems
    Sunrise Systems Summit, United States

    1 week ago

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    Description

    Job Description:

    Minimum 50% onsite required every week (Candidate is supposed to align the onsite days with manager and be available onsite when manager requests)

    REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:

    • Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE) and Recipe Authoring/Validation.
    • Ability to work extended hours or a modified work schedule to assist manufacturing operations support model, including 12x7 on-call support rotation
    • Knowledge of cGMP, GxP, GAMP, and SDLC regulations, including 21CFR part 11 electronic records and electronic signatures, and good documentation practices with the ALCOA+ principles of data integrity, risk-based approaches to validation, Computer Software Assurance (CSA) principles
    • Understanding the concept of Critical thinking for Computerized Systems
    • Familiar with the development of CSV documentation (Validation Plans, Requirements, Design / Configuration Specifications, Test Scripts [IQ/OQ/PQ/UAT], Summary Reports, Trace Matrices, SOPs)
    • Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods
    • With advanced technical document writing and time management skills, including ability to prioritize and manage expectations
    • Operate effectively and with minimal supervision, within a team or independently, performing projects and related duties

    Education and Experience:

    • Bachelor's degree in a life sciences, engineering or technology discipline required
    • Minimum of 2+ years relevant work experience required preferably in a pharmaceutical manufacturing environment.
    • An equivalent combination of education, experience and training may substitute.


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