Quality Assurance Inspector

Job Title: QA Inspector Location: Medina, NY Duration: 06 + Months ( Contract/Temp with the possibility of extension) Shift: 1st Shift (Monday–Thursday: 5:30 AM – 4:00 PM) Friday overtime as needed Hours: 40 hours per week Pay Range: $23/hr to $25/hr Job Description: We are seeking a detail-oriented Final QA Inspector to join a manufacturing quality team in an FDA-regulated environment. In this role, you will perform final quality inspections, review production documentation, verify product compliance, and ensure products meet quality standards before release. The ideal candidate has experience working in a regulated manufacturing environment and is knowledgeable in cGMP and FDA requirements. Key Responsibilities: Perform final inspection of production documentation to ensure all manufacturing and testing requirements have been completed. Inspect finished products for visual quality, labeling accuracy, and compliance with release specifications. Review device history records and manufacturing documentation for completeness and accuracy. Approve product release within the applicable electronic systems. Verify there are no open quality issues or nonconformances prior to product release. Document inspection findings, defects, and rework activities accurately. Process and close nonconformance records following established procedures. Support containment activities for nonconforming products during quality investigations. Ensure compliance with quality procedures, process controls, and manufacturing standards. Recognize quality issues and escalate concerns when necessary. Perform inspection and release of service parts as required. Complete additional quality-related duties as assigned. Required Qualifications: High School Diploma or GED. Experience working in an FDA-regulated manufacturing environment. Knowledge of Current Good Manufacturing Practices (cGMP). Understanding of FDA quality requirements. Experience performing quality inspections in a manufacturing setting. Strong attention to detail and documentation accuracy. Basic computer, data entry, and Microsoft Office skills. Experience using measurement and inspection equipment. Strong verbal and written communication skills. Ability to work overtime and flexible hours when needed. Preferred Qualifications: Experience in medical device, pharmaceutical, biotechnology, or other regulated manufacturing industries. Experience reviewing Device History Records (DHR). Experience with Manufacturing Execution Systems (MES) or ERP systems. Familiarity with nonconformance documentation and quality systems. Physical Requirements: Ability to sit, stand, and walk for extended periods. Good hand-eye coordination and manual dexterity. Ability to lift and carry up to 25 pounds. Ability to push or pull up to 5 pounds. Ability to perform detailed visual inspections, including identifying defects and distinguishing colors. (LH-R2) Employment Type: Full Time Salary: $23 - $25 Hourly Bonus/Commission: No