MedTech Quality Assurance Lead

Regulatory Jobs; Memphis (TN); On-site; USD 75,000 - 95,000; Full time

Job summary

Globus Medical is seeking a Team Lead to organize and guide the quality inspection team, collaborating with engineers on set-up and calibration tasks. You will document results, drive methods for quality assurance, and push for performance improvements to meet department and company goals.

The role emphasizes maintaining compliance with FDA, ISO 13485, and related standards, while supervising calibrations, reworks, and deviations. Strong communication and teamwork are essential.

Qualifications

• Typical requirement: 6+ years of related experience.
• High school diploma or equivalent is required.
• AA in a technical field is preferred.
• Strong written and oral communication skills are essential.
• Excellent organization and documentation skills are required.
• Advanced ability to work in a team and drive daily objectives.
• Familiarity with quality systems standards (ASME Y14.5M, ISO 13485) is expected.

Responsibilities

• Ensures consistent application of quality procedures for compliant inspection of product.
• Sets daily, weekly, and monthly team goals to meet corporate goals and regulatory requirements.
• Partners with Quality Engineering to qualify and validate inspection equipment and processes.
• Keeps accurate records for calibrations, reworks and deviations.
• Performs other duties as assigned.
• Adheres to Code of Conduct and company policies and ensures compliance with laws and regulations.

Skills

Strong written and oral communication

Teamwork

Documentation skills

Organization

Discipline

Education

High school diploma or equivalent required

AA in a technical field preferred

Tools

ASME Y14.5M

Blueprint reading

FDA regulations

ISO 13485

Job description

Globus Medical is seeking a Team Lead to organize and guide the quality inspection team, collaborating with engineers on set-up and calibration tasks. You will document results, drive methods for quality assurance, and push for performance improvements to meet department and company goals.

The role emphasizes maintaining compliance with FDA, ISO 13485, and related standards, while supervising calibrations, reworks, and deviations. Strong communication and teamwork are essential.