Description
SUMMARY Highly motivated Quality Professional with over 15 years' combined working knowledge in Quality System Regulations (QSR), Quality Management System (QMS), FDA Inspection Readiness, and Systems Based Auditing with varied cGMP, cGLP, Nonconformance and CAPA Management experience. Experience in regulated environments for Pharmaceutical, Medical Device, Biologics and Bio-Chemical industries. Demonstrated strengths in organization, analytical thinking, attention to detail, compliance and process improvement problem resolution. Adept at multi-tasking and meeting deadlines. Effective in creating environments to streamline validations, corrective action plans and effectiveness maintenance for process improvement initiatives. Dependable, hardworking, and resourceful. Excellent interpersonal and communication skills with individuals at all levels.
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