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An error has occured. Please close this dialog and try again. Please complete the entire form below to apply. First Name* Last Name* Email* Phone* (Phone Numbers Only) Cell Phone* (Phone Numbers Only) City* State of Residence* Select a state... Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware District Of Columbia Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming Skills* Software Sales Quality Control Office and Administrative Marketing Manufacturing and General Management Maintenance Machine Operator LI-Manufacturing Legal Welder Warehouse Transportation Other Area(s) Work Preference* Please select an option... Manufacturing Clerical Please complete the entire form below to apply. Resume (optional) By registering or applying with Belflex you agree to receive text messages about job offerings we have. You may opt out at any time. Apply Now Thank you for applying, your local branch will be reaching out to you shorty. * Required field. Belflex Staffing has partnered with a manufacturing facility located in Walton, KY. They are currently have an opening for a Validation Specialist.Pay: $25.00 and up depending on experience.
Hours: 7:00 am – 3:30 pm
Job Summary:
Responsible for developing, preparing, executing and overseeing the execution of and the revising of validation
procedures/protocols to ensure that there is sufficient documentation to support the manufacturing of a product in accordance with appropriate regulatory agency requirements, customer expectations, and internal company standards. Compiles and analyzes validation data, prepares reports and makes recommendations. Performs all tasks in accordance with cGMP guidelines and quality standards. Must be able to work in a team environment and possess team-based problem-solving skills. Must be results focused and oriented toward accomplishment of organizational goals. Must be able to work flexible hours to include overtime when needed.
Responsibilities:
Ensure all processes and methods critical to product quality are appropriately qualified, validated and documented. Actively participate during all phases of validation including documents for IQ/OQ. Review engineering drawings. Analyze data and provide recommendations for improvements. Maintain system that tracks validation records. Write, review and approve validation strategies, protocols and reports. Review validation packages for completeness and accuracy, sound rationale, compliance with policies and procedures, and accurate data analysis. Establish priorities and schedule activities to ensure timelines and milestones are met. Some administrative activities may be required as needed.Qualifications:
Bachelor’s Degree in Science, Business Detail oriented Proficient in Math Basic communications and writing skills in English Ability to interact and work with team members Ability to communicate knowledge to team Must have knowledge of current industry expectations of validation requirements forIQ/OQ/PQ/Cleaning/Equipment validations Ability to handle multiple projects and deliver reports in a timely manner Ability to determine, present, and defend project requirements and status Must have knowledge of all current GMP requirements Ability to communicate written and verbally #420
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