Quality Control Technician - GMP

Quality Control Technician - GMP

Location: Pomona, CA

Onsite Flexibility: Onsite

Contract Details

• Position Type: Contract
• Contract Duration: 6 months
• Pay Rate: $25.90 / Hour (USD)
• Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Job Summary

The position of QC Technician II is within the Toxicology Business Unit located in Pomona, CA. This position will support QC functions within a Drugs of Abuse test manufacturing facility. The position will primarily be focused on performing in-process and finished products QC testing, documenting test results to ensure the quality and functionality of manufactured products.

Key Responsibilities

• Perform and document incoming, in-process, and final QC testing of in-vitro diagnostics devices to meet compliance requirements including ISO, FDA, and international regulations.
• Familiarity with all aspects of the product and be able to identify defects.
• Crosstrain on all processes in QC lab.
• May train new staff on processes.
• Able to solve process-related questions/problems.
• Use Agile to issue quality incidents; perform root cause investigation and write investigation report.
• Perform validation study or other appropriate analyses for current or new product/new features of the product.
• Prepare adulteration controls and DOA controls as needed.
• Be able to use an analytical balance, optical comparator, vacuum chamber, caliper, gauges, and other tools to perform QC testing or measurements.
• Ensure timely release of product.
• Ensure cleanliness of the QC lab.
• Assist the head of QC department with any necessary tasks.
• Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.
• Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices; builds productive internal/external working relationships.
• Carries out duties in compliance with established business policies.
• Other duties as assigned, according to the changing needs of the business.

Required Skills

• Ability to follow detailed instructions, maintain accurate records and notes, and carry out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices.
• Good written and verbal communication skills.
• Experience working in a GMP environment.
• Intermediate knowledge of a variety of lab equipment and their operation.
• Intermediate knowledge of MS Office and manufacturing systems.

Preferred Skills

• Experience working with semi-automated equipment.
• Medical device manufacturing preferred.
• Knowledge of regulations (FDA, ISO, OSHA, etc.).
• Be able to prioritize and handle multiple tasks and responsibilities, with attention to detail.

Education Requirements

• High school diploma required.

Required Experience

• Two to five years of laboratory experience.

Benefits

• Medical, Vision, and Dental Insurance Plans
• 401k Retirement Fund

About the Client

This client is a leading healthcare innovator dedicated to improving lives worldwide through a diverse portfolio of medical devices, diagnostics, and nutrition products, with a global presence spanning more than 160 countries. The organization operates across medical devices, diagnostics, nutritional products, and pharmaceuticals, employing biomedical engineers, clinical scientists, regulatory affairs specialists, and commercial operations professionals. With more than 140 years of medical innovation, the company is a certified Great Place to Work and offers cross-functional teams, international exposure, and a mission-driven culture grounded in inclusion and innovation giving professionals the opportunity to make a measurable difference in global health outcomes.

About GTT

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

Job Number: 26-10452 Industry: Manufacturing & Operations

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