Quality Supervisor Incoming

Quality Incoming Supervisor Job Location:

Athens, TX Schedule:

Monday-Friday, 7:00 AM - 4:00

PM Pay:

$70,000 salary

DOE Position Summary:

Remedy Staffing is seeking a Quality Incoming Supervisor for an immediate opportunity in Athens, TX. This role will oversee incoming inspection operations within a regulated manufacturing environment, ensuring materials and products meet strict quality standards.

Key Responsibilities:

Supervise and lead incoming quality inspection staff, including training, coaching, and performance management Schedule and prioritize daily inspection activities to meet production demands Oversee inspections of raw materials, components, and finished products using defined quality standards Review Device History Records (DHRs) for compliance prior to product release Identify and develop top-performing inspection staff to support in-process audits Ensure accurate documentation of inspection results and quality records Coordinate equipment calibration and maintain inspection tools and systems Perform root cause analysis on inspection errors and implement corrective actions Maintain adherence to Quality Management Systems (QMS) and documentation standards Act as the communication bridge between leadership and quality teams Apply Today This is a great opportunity for a driven quality leader to step into a high-impact supervisory role. If you have experience in quality inspections, QMS, and team leadership, we encourage you to apply today. Bachelor's degree OR 5+ years of relevant experience (or equivalent combination) Minimum of 2 years supervisory experience Experience with MRP systems (QAD or similar preferred) Strong written and verbal communication skills Proficient in Microsoft Office (Word, Excel, Access) Highly detail-oriented with strong time management skills Strong leadership skills with the ability to assess, develop, and coach inspection teams Experience building and training high-performing inspection personnel Knowledge of medical device or pharmaceutical QMS environments Technical expertise in inspection methods (attribute and variable) Proven problem-solving and root cause analysis experience Experience in medical device manufacturing Knowledge of Good Documentation Practices (GDP)