Manage, write, investigate, review and approve deviations, CCR's CAPA's, product complaints. Manage metrics. Help out in other areas of quality assurance as required.
Understanding of Good Manufacturing and Laboratory Practices, FDA regulations, SOPs, and current compliance standards. Attention to detail. Experience in Root cause analysis (5 WHY's, Fishbone) Good technical writing skills This position requires a B.S. degree and 2- 4 years experience in pharmaceutical manufacturing or 4-8 years of equivalent experience
Source: Job Diva – Job Listing