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Quality Assurance Specialist - Pharma

Company: Experis
Location: Boston
Posted on: August 24, 2019

Job Description:

Our client in Boston, MA, a leader in drug discovery and development, is seeking a Quality Assurance Specialist to join a fast moving and critical team for a 6 month contract. Duties - Support daily activities related to processing and maintenance of controlled GMP documents associated with document management functions( procedures, specifications, reports and batch records). - Support activities related to the processing of training records associated with the training program by creating courses in electronic training system. - Assist with the development and implementation of annual site training plan. - Assist with improvements to applicable standard operating procedures and electronic systems related to document control, GMP training and quality systems. - Assist with reviews and asses deviations participating in root cause investigation, tracking, follow up and reportingtrending. - Assist with analyzing quality system data to measure key performance indicators, identifies areas for continuous process improvements and risk mitigation, complies and presents analyses at Quarterly Management Review meetings, proposes appropriate CAPA. - Assist in creating documents including Standard Operating Procedures. Provide support for internal audits for GMP compliance. Required Skills - 9+ Years of QA experience in the Pharmaceutical industry - GMP experience - CAPA experience - Document Control and Document Management experience - Experience conducting Internal Audits - Experience working with Batch Records - Mitigation and Process Improvement Experis is an Equal Opportunity Employer (EOEAA)

Keywords: Experis, Leominster , Quality Assurance Specialist - Pharma, IT / Software / Systems , Boston, Massachusetts

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