Validation Engineer (Lynchburg, VA)

Company: Jobleads
Location: Lynchburg
Posted on: May 3, 2021

Job Description:

Validation of productmanufacturing and packaging systems. This includes IQ/OQ/PQ, process validation and cleaning validation. Develop company validation standards. Support quality programs such as change control, calibration and technical releases. Accountabilities Perform all company validation functions related to manufacturing, raw materials, packaging, testing, and distribution of our products and raw materials, including writing protocols and final reports, reviewing testing methods, and analysis of data. Moderate direct impact on profitability results from maintaining proper adherence to validation and stability guidelines. Responsibilities Develop and write validation policies, procedures and protocols. Perform IQ/OQ/PQ, cleaning and utilities validation. Work closely with Engineering on new equipment specifications and engineering changes as related to process and cleaning validation. Evaluate, identify and develop current company validation and stability standards to meet global requirements and current industry standards. Supervise, coordinate and provide QA oversight for assembling and issuing New Product Technical releases prior to initial release of product to the market. Supervise, coordinate and provide QA oversight for the Fleet Laboratories calibration program. Supervise, coordinate and provide QA oversight for line/ship tests. Supervise, coordinate and provide QA oversight for the change control process at Fleet Laboratories. Provide technical support on process investigations, quality improvement and CAPA activities (corrective and preventive action). Participate in training and instruction of departmental supportive personnel and provide technical leadership to the department. Provide technical support to a variety of corporate and international programs. Perform other related duties as required. Provides oversight for the calibration program. Use considerable judgment skills to troubleshoot and rectify any problems in testing and processing of products while conforming to company standards for product quality. Perform FATs as needed and provide technical expertise for acceptance test on site PHYSICAL REQUIREMENTS : QUALIFICATIONS : Associates of Science and/or BS degree in Math, Science, Engineering or related field Minimum of 10 years' experience in pharmaceuticals or other GMP industry Minimum of 5 years' experience in Validation and/or Technical Services Experience with equipment qualification is recommended Ability to travel by car, rail and air. Prestige is an Equal Opportunity Employer Search Firm Representatives - Please read carefully: PRESTIGE CONSUMER HEALTHCARE does not accept unsolicited assistance from search firms. Please, no phone calls or emails. All resumes sent by search firms to any employee at Prestige Consumer Healthcare via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Prestige Consumer Healthcare. No fee will be paid in the event the candidate is hired by Prestige Consumer Healthcare as a result of the referral or through other means. Thank you for your cooperation. Apply For This Position Upload Resume Files must be less than 5 MB.Allowed file types: pdf doc docx. Beware of Cyber Job Scammers The jobs you see posted here on this website are the ONLY positions for which Prestige is currently recruiting candidates. Click here for more information .

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