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Premier Life Sciences VALIDATION ENGINEERS in South Plainfield, New Jersey

Design, develop and oversee validation components using Six Sigma and Minitab. Write and execute engineering change orders related to Corrective and Preventive Actions (CAPA). Analyze and rationalize CAPAs, Nonconformances (NCs), observations, and failure investigations. Create Master Validation Plans for various products, validation protocols, summaries, and approvals. Develop test methods and process validation like IQ/OQ/PQ. Perform root cause and gap analysis. Create and update Failure Mode and Effect Analysis (FMEA) for new implants and instruments. Master’s degree in Science, Technology, Biotechnology, or Engineering (any) is required. Work location: South Plainfield, NJ and various unanticipated locations throughout the U.S.Email Resume to HR Dept., Premier Life Sciences, LLC., at hr@premierlifesciences.com

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