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    Validation Engineer - Beloit, United States - Automated Systems

    Automated Systems
    Automated Systems Beloit, United States

    2 weeks ago

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    Description
    Job Description

    Job Description

    Validation Engineer
    Contract: 6+ months duration with possible extensions

    Location:
    Beloit, WI – onsite

    Automated Systems, Inc.

    is seeking a dedicated Validation Engineer to work with one of our leading pharmaceutical manufacturing clients located in Beloit, WI.

    In this role, the Validation Engineer will be assisting in establishing Commissioning and Qualification (C&Q)

    policies/strategies,

    lead specific C&Q activities for pharmaceutical manufacturing equipment and processes, ensuring compliance with quality

    standards/requirements,

    and industry standards (FDA, EMA, ISO, ICH, etc.). All projects and duties will be completed in compliance with applicable cGMP, FDA, and all other regulatory agencies standards.
    Job Role Duties and Responsibilities
    Assists in the change management of facilities, utilities, systems, equipment (FUSE), and processes.

    Able to drive C&Q project completion and compliance in a challenging and fast-moving environment in a timely and efficient manner.

    Assists in developing and managing the C&Q Programs/Processes including generating and maintaining site and project C&Q plans, overseeing C&Q

    schedules/activities,

    and coordinating various C&Q activities with cross functional teams.

    Work with cross-functional teams in design reviews, impact assessments, generation of requirements, risk assessments, and other identified C&Q deliverables.
    Education, Experience and Skill Requirements
    ·

    Bachelor's degree in Engineering or a Science-related field with 3+ years of progressive experience in the pharmaceutical industry with at least 2 of those years acting in a

    Qualification/Validation

    role; or equivalent combination of education and experience.

    ·

    Experience working with current validation principles, standard concepts, practices and procedures, and

    ·

    Relevant working experience with the requirements and regulations in a cGMP regulated environment is necessary.

    ·

    Demonstrated proficiency in five or more validation areas required.

    ·

    Experience with Statistical Analysis preferred.

    ·

    Strong collaboration, communication, and presentation skills required.

    ·

    Expert-level proficiency with Microsoft Office (Word, Excel, PowerPoint, and Outlook) is required.
    Company Description We are a dynamic, project oriented consulting company offering individuals a wide variety of technical challenges. We are currently experiencing rapid growth, and are in need of talented individuals. ASI offers top wages and excellent benefits. ASI is an equal opportunity employer.

    Company Description

    We are a dynamic, project oriented consulting company offering individuals a wide variety of technical challenges. We are currently experiencing rapid growth, and are in need of talented individuals. ASI offers top wages and excellent benefits. ASI is an equal opportunity employer.
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