Quality Control Technician

Globus Medical • San Antonio, TX

7d

About The Position

The Quality Control Technician works within the Quality Department and in-house manufacturing to support quality-system compliance and continuous improvement. The role oversees and participates in developing, documenting, monitoring, and maintaining quality systems to ensure conformance with regulatory requirements and company policies and procedures throughout manufacturing. The technician conducts quality-control testing and inspections, prepares test reports, supports equipment qualification, monitors controlled environments, reviews processing and sterilization records, and helps coordinate equipment calibration and preventive maintenance. Other duties and responsibilities may be assigned as necessary.

The role requires adherence to company and industry codes of conduct, applicable policies, and governmental laws and regulations in the United States and internationally. The employee represents the company professionally and maintains ethical and socially responsible conduct. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Requirements

• Minimum 2 years of experience in Quality Control.
• Knowledge of GMP regulations preferred.
• Knowledge of Microsoft Word, PowerPoint, and Excel.
• Strong typing skills.
• Strong analytical skills and problem-solving techniques.
• Excellent communication and writing skills.
• Ability to work as a flexible team player in a deadline-driven environment.
• Ability to occasionally sit, climb or balance, reach above shoulder level, push or pull, and stoop, kneel, crouch, or crawl.
• Ability to occasionally lift and move or carry up to 30 pounds.
• Vision abilities including close, distance, color, and peripheral vision, depth perception, and ability to adjust focus.

Nice To Haves

• Bachelor’s degree preferred.
• Knowledge of GMP regulations preferred.

Responsibilities

• Perform quality-control testing on manufacturing supplies, in-process materials, and finished products, including DBM, residual moisture, and peel testing as needed.
• Perform in-process and final product inspections.
• Draft test reports for tests performed.
• Participate in qualification of new manufacturing equipment.
• Perform viable and non-viable particulate environmental monitoring in cleanrooms.
• Monitor temperature, pressure, and humidity in controlled environments.
• Identify non-conformances and areas for improvement.
• Inspect and approve product labeling.
• Help coordinate facility equipment calibrations and preventive maintenance.
• Review cleaning logs and steam and ETO sterilization runs.
• Complete personnel environmental monitoring.
• Participate in continuous-improvement functions and implement changes.
• Review processing records, test results, certifications, and other documentation as needed.
• Adhere to the company Code of Conduct, the AdvaMed Code, the MedTech Code, and other company policies.
• Complete introductory and annual training and maintain knowledge of compliance requirements relevant to the role.
• Represent the company professionally and uphold ethical business practices and socially responsible conduct in interactions with employees, customers, suppliers, and other third parties.
• Perform other duties and responsibilities as necessary.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level