Job Opening: Quality Supervisor – Incoming
Description
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)