Quality Engineer II - (Trenton, GA)

The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System qualifications are adhered to for medical device manufacturing/operations in accordance with applicable Regulatory and Standards qualifications for compliance. Provide work direction for 1-3 Technicians/Inspectors. Key Accountabilities and Responsibilities Adheres to Company Core Beliefs and all safety and quality qualifications including, but not limited to: Quality Management Systems (QMS), Environmental Management Systems (EMS), U.S. Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and other regulatory qualifications. Support regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality.