Microbiology Lab Technician

Overview Talent Title: Quality engineer Location: Plymouth, MN Duration: 24 Months Description: Quality engineer experienced with internal or external auditing to internal QMS requirements; understands 21 CFR 820, ISO 13485, and CGMP Regulations. Responsibilities Understand QMS requirements at a detail level Review product and QMS documentation to evaluate compliance Maintain an internal audit schedule Assist in communicating internal audit agendas and scheduling Participate in internal audits Generate Internal Audit reports Review and approve product and QMS work products as required General Quality Engineer tasks as required Qualifications Experience with internal or external auditing to QMS requirements Knowledge of 21 CFR 820, ISO 13485, and CGMP Regulations Seniority level Mid-Senior level Employment type Contract Job function Quality Assurance Industries Medical Equipment Manufacturing Pharmaceutical Manufacturing #J-18808-Ljbffr