Quality Associate
▪ Managed and directly supervised assigned personnel in providing quality oversight and achieving defined company goals ▪ Collaborated with supervisors and management on a daily basis to develop courses of action to correct identified risks and areas of non-conformance on the manufacturing floor▪ Supported audits of various reports such as internal protocols, validations, and external GMP/GDP inspections by the FDA and other regulatory health agencies▪ Worked to write, review, analyze and revise written Standard Operating Procedures (SOPs) to meet Corporate, Divisional, and Local requirements