On-Site Quality Control Supervisor & Lead Inspector

Arterex

Mansfield (MA)

Presencial

USD 64.000 - 72.000

Jornada completa

Hace 3 días
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Descripción de la vacante

NextPhase Medical Devices LLC seeks a Quality Control Inspector Supervisor in Mansfield, MA to lead quality assurance activities and ensure materials meet standards while maintaining production flow. The role supervises inspectors, coordinates calibration, and initiates nonconforming material reports.

Requires 5–8 years in quality control and familiarity with FDA Quality System regulations. On-site position with full-time hours; the candidate will collaborate across design, purchasing and

Formación

  • 5–8 years experience in Quality Control Inspection.
  • Knowledge of quality standards and current industry practices.
  • Excellent documentation, writing and communication skills.
  • Familiarity with FDA Quality System Regulations (QSR).
  • Ability to coach and lead an inspection team.

Responsabilidades

  • Supervise and coordinate activities related to quality control including staffing, scheduling, coordinating, and planning the TQM program.
  • Supervise personnel responsible for inspection and reports on material, processes, and incoming products to ensure compliance with quality standards.
  • Communicate standards and training; coordinate programs related to product quality.
  • Document discrepancies and follow up on corrective actions.
  • Schedule calibration and preventive maintenance.
  • Remove equipment from service when needed due to calibration issues.

Conocimientos

Quality Control
Inspection
Leadership
Documentation
FDA QSR familiarity

Educación

ASQ Certification

Descripción del empleo

NextPhase Medical Devices LLC seeks a Quality Control Inspector Supervisor in Mansfield, MA to lead quality assurance activities and ensure materials meet standards while maintaining production flow. The role supervises inspectors, coordinates calibration, and initiates nonconforming material reports.

Requires 5–8 years in quality control and familiarity with FDA Quality System regulations. On-site position with full-time hours; the candidate will collaborate across design, purchasing and

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