Delta V Automation Engineer - Athens, United States - Insight Global

    Insight Global background
    Description
    An employer is seeking a Automation Engineer with a proven track record in computer system validation for DeltaV. This will be an ongoing contract for medical device company in the Athens, GA location.

    The ideal candidate would like to expand their skills within a highly regulated industry and be open to on site work 4-5 days a week.

    This role will be in support of Emerson DeltaV DCS and main responsibility is to quality assurance plans, verification plans, validation plans, and standard operating procedures as well as conduct risks assessments and participate in Quality/Regulatory audits.

    The automation engineer must have a background in PLCs,


    Emerson DeltaV DCS and some other computer system validation experience will suffice with the proper amount of programming, coding or batching.

    Experience with automation, commissioning, qualification or operations in a cGMP environment will allow for this Automation Engineer to hit the ground running.


    We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day.

    We are an equal opportunity/affirmative action employer that believes everyone matters.

    Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances.

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    Required Skills & Experience

    3+ years' experience computer system validation (CSV) experience with process control in DeltaV DCS

    3+ years of validation experience with other DCS and PLC

    3+ years automation, commissioning, qualification or operations in a cGMP environment in Delta V

    Direct experience developing validation protocols and execution of protocols

    Experience creating validation master plans and performing risk assessments.

    Comfortable working on site 4 days a week and overseeing plant floor operations

    Nice to Have Skills & Experience

    Knowledge of current industry standards such as GAMP5 and ASTM E2500.

    Medical device industry knowledge

    Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching.

    Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.