Quality Control Supervisor

At Tactile Medical, we specialize in developing at‑home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses.

• Supervise, coordinate, and prioritize daily activities of Quality Inspectors and Quality Technicians responsible for nonconformance, product returns and receiving inspection to meet production and quality objectives
• Provide training, coaching, and performance feedback while ensuring adherence to procedures and Good Documentation Practices
• Serve as a hands‑on leader by acting as a backup and float across quality inspection and technician functions
• Maintain and monitor quality metrics associated with receiving inspection and nonconformance to ensure performance targets are met
• Manage receiving inspection and returned product queues to ensure priority items are completed in a timely manner and target metrics are maintained
• Perform and support incoming, in‑process, and final inspection, including testing, measurement, and product evaluation
• Lead and support non‑conforming material processes, including documentation, investigation, disposition, and escalation
• Lead and support processing and investigation of product returns, ensuring proper documentation and analysis
• Support development and review of procedures associated with Quality Control
• Ensure compliance with QMS, HIPAA, and regulatory requirements (e.g., 21 CFR 820, ISO 13485)
• Identify and lead continuous improvement initiatives using data analysis, trend monitoring, and operational insights to identify areas of improvement and lead continuous improvement projects
• Other duties as assigned

• Associate’s degree or equivalent work experience in a related discipline
• Minimum of 1 year of leadership or lead experience or demonstrated leadership capability
• Minimum of 5 years’ experience working in a regulated manufacturing environment (at least 2 years of that time must be in a medical device under ISO 13485)
• Strong working knowledge of inspection, testing, and quality processes
• Familiarity with Excel for compilation/trending of data
• Knowledge of GXP, 21
  
  CFR, ISO, QSR and other applicable regulations, standards, directives and guidance

• ASQ certification (CQT, CQI or similar)
• Experience with ERP/MRP systems such as Net Suite
• Experience with eQMS software such as Grand Avenue Knowledge & Skills
  • Working knowledge of quality inspection, testing, nonconformance, and product return processes
  • Knowledge of QMS and regulatory requirements, including 21 CFR 820, ISO 13485, and Good Documentation Practices
  • Ability to lead, coach, and prioritize daily work for inspectors and technicians
  • Strong analytical, problem‑solving, and data trending skills using Excel and quality metrics
  • Effective communication and collaboration skills with a continuous improvement mindset
  Benefits

  Our total compensation package includes medical, dental and vision benefits, retirement benefits, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness benefits and discounts. Benefits may be subject to generally applicable eligibility, waiting period, contributions, and other requirements and conditions.

  US Pay Range: $61,500 — $86,205 USD