Manufacturing Quality Manager

Quality Inspection Manager Temp to hire Contract Payrate- $55 to 60/hr on W2 Conversion Salary going full time around $111,000 plus benefits Candidate should be flexible with the work hours Interview Process: 2 rounds -1st round 15/30 minute TEAMS call -2nd round will be in person and will be a panel interview Location: Will work at 2 locations Lewisville TX Mon-Wed and Friday. DALLAS TX 75220 - Thursday Snapshot: - 7+ years of experience in FDA‑regulated consumer products, with 2+ years leading teams. - Bachelor’s degree in engineering or a science discipline (Master’s in Engineering preferred). - heavy system compliance, ops and production based, pharma mfg. exp. is good, identifies what is and is not quality, QMS and systems knowledge (Agile PLM, LIMS and Warehouse management/JDE - manages directly the team at ASRS (2 people) which is responsible for QI for received contract manufactured product - oversees Group Leader at R3 whose team (15 people) is responsible for inspecting ingredients and components received, and finished goods being mfg. at R3 - Strong technical expertise in cGMPs, quality audits, statistics, testing, and manufacturing operations; ASQ CQE or CMQ/OE preferred. Manager, Quality Inspection In this role, you’ll lead the Quality Inspection team responsible for ensuring every component, raw material, and finished product meets our rigorous global standards. You’ll guide a talented team, partner closely with cross‑functional groups, and influence quality excellence across internal manufacturing and external contract partners. What You’ll Do · Lead and develop the Quality Inspection team, setting clear goals, coaching talent, and maintaining a safe, positive, and high‑performance environment. · Oversee inspection and sampling of components, raw materials, semi‑finished, and finished goods produced in Lewisville and by U.S. contract manufacturers. · Provide expert technical guidance on defect classification, AQL sampling plans, and Good Manufacturing Practices. · Drive quality improvements by identifying issues, analyzing data, recommending solutions, and supporting corrective and preventive action plans. · Communicate test results and technical insights to internal partners and external suppliers with clarity and urgency. · Ensure non‑conforming materials are properly segregated, investigated, dispositioned, and removed from the supply chain as needed. · Serve as the inspection subject‑matter expert for global Quality teams. · Maintain compliance with FDA regulations, cGMPs, and quality standards while managing departmental programs, procedures, equipment, and budget. What You Bring · 7+ years of experience in FDA‑regulated consumer products, with 2+ years leading teams. · Bachelor’s degree in engineering or a science discipline (Master’s in Engineering preferred). · Strong technical expertise in cGMPs, quality audits, statistics, testing, and manufacturing operations; ASQ CQE or CMQ/OE preferred. · Proven ability to troubleshoot complex issues, lead change, and drive continuous improvement. · Excellent communication, leadership, and project management skills. · Working knowledge of modern lab instrumentation and inspection methodologies. · Ability to stand/walk for extended periods and lift up to 20 lbs. · Willingness to travel up to 10%.

Created: 2026-03-12