Quality Specialist

Overview

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions.

Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible.

The Quality Specialist will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies and procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. As a contributor to the quality engineering organization, this professional will be self‑motivated and characterized as an excellent problem‑solver.

This person will play an integral role in maintaining and improving the quality management system, product quality, and manufacturing process quality.

• Coordinate and manage the calibration program for inspection, measuring, and test equipment in accordance with applicable control of monitoring and measuring devices procedures
• Maintain the calibration database, including equipment identification, calibration intervals, status, tolerances, and calibration methods
• Ensure all equipment is calibrated on schedule using approved internal procedures or qualified external calibration suppliers
• Review calibration certificates for completeness, accuracy, traceability to national or international standards, and acceptance criteria
• Facilitate the investigation and documentation of out‑of‑tolerance conditions, including equipment impact assessments and product evaluations
• Ensure equipment is properly labeled with calibration status and segregation of non‑calibrated or out‑of‑tolerance equipment
• Support audits and inspections by providing calibration records, logs, certificates, and program procedures
• Coordinate equipment repairs, adjustments, re‑calibration, and retirement as required
• Trend calibration data and metrics to support continuous improvement
• Assists with maintenance of the Quality Management System by ensuring documents are approved, issued, revised, archived, and withdrawn in compliance with applicable documentation and change control procedures
• Supports training and competency requirements by creating, assigning, and managing role‑based training curricula aligned with job functions and controlled document changes
• Contributes to nonconformance activities
• Collaborate with cross‑functional partners—Product Development, Operations, Supply Chain, Regulatory and Field Service—to clarify requirements, close gaps, and drive timely approval of documentation packages
• Assist in preparation for external and internal audits by organizing documentation, gathering objective evidence, and responding to auditor requests. Support timely closure of audit observations.
• Provides written and oral reports to supervisor or other management personnel to keep them informed of activities and results
• Adheres to the letter and spirit of the company Code of Conduct, the Adva Med Code, Med Tech Code, and all other company policies.
• Ensures compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role.
• Represents the company in a professional manner and upholds the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties

• High School diploma or equivalent required
• 0‑2 years' experience in quality assurance; experience in the medical device industry preferred
• GMP and ISO experience with a focus on control of monitoring and measuring devices
• Proficiency in using Microsoft Office products
• Must be a team player capable of working in a deadline‑dictated environment
• Excellent verbal and written communication skills
• Self‑starter

Required to sit; climb or balance; and stoop, kneel, crouch or crawl. Required to regularly lift and/or move up to 10 pounds, and occasionally lift and/or move up to 25 pounds. Required to possess specific vision abilities, including: close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus.

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.