Quality Control Team Lead - MedTech Excellence

NML Medical

Memphis (TN)

Presencial

USD 75.000 - 110.000

Jornada completa

Hace 4 días
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Descripción de la vacante

Globus Medical in Memphis, TN seeks a Team Lead, Quality Control to organize and guide a quality inspection team during the 3 PM–12 AM CST shift. You will work with engineers on setup, calibration, rework, and documentation to ensure compliant QA outcomes.

The role requires 6+ years in QA, a technical background, strong communication, and familiarity with ISO 13485 and FDA standards. Join us to help deliver innovative musculoskeletal solutions.

Formación

  • Typically requires a minimum of 6+ years of related experience.
  • High school diploma or equivalent required.
  • AA in a technical field preferred.
  • Strong written and oral communication skills.
  • Good organization and documentation skills.
  • Advanced ability to work effectively in a team environment and drive performance of daily objectives.
  • Intermediate proficiency in ASME Y14.5M and blueprint reading.
  • Perform duties in compliance with FDA and ISO 13485 standards.

Responsabilidades

  • Organizes and leads quality inspection team through QA operations.
  • Sets daily, weekly, and monthly goals to meet corporate and regulatory requirements.
  • Partners with Quality Engineering to qualify inspection equipment and processes.
  • Keeps accurate records for calibrations, reworks, and deviations.
  • Represents the company in a professional manner and maintains ethical standards.

Conocimientos

Quality inspection leadership
Blueprint reading
ASME Y14.5M
Team leadership
Data collection & analysis

Educación

High School Diploma or Equivalent
AA in a technical field preferred

Herramientas

Regulatory compliance

Descripción del empleo

Globus Medical in Memphis, TN seeks a Team Lead, Quality Control to organize and guide a quality inspection team during the 3 PM–12 AM CST shift. You will work with engineers on setup, calibration, rework, and documentation to ensure compliant QA outcomes.

The role requires 6+ years in QA, a technical background, strong communication, and familiarity with ISO 13485 and FDA standards. Join us to help deliver innovative musculoskeletal solutions.

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