Quality Control Technician – Entry Level

Job Summary

Responsible for the implementing of quality inspection plans for in-process production and final release. Responsible for the timely closure of Device History Records for in-process Finished Goods – including assistance with the investigation and closure of Non-Conforming Material Reports at the Interventional Specialties Manufacturing facility, Mannford, OK.

Principal Accountabilities

• Schedules and implements quality inspection plans for in-process production and final release.
• Performs final DHR release for in-process finished goods.
• Provides supplemental quality support to ongoing projects and technical service requests.
• Affords assistance with the investigation and closure of applicable Non-Conforming Material Reports.
• Works with management to enhance the quality system with the Mannford facility.
• Provides proactive feedback to Manufacturing and Material personnel on quality issues.
• Applies analytical and problem-solving techniques in the normal course of daily activities.
• Knowledge of FDA, ISO, EN, QSR (GMP’s), GLP and other regulatory requirements related to the manufacture of medical devices.
• Knowledge of statistical techniques as related to sampling.
• Other duties as assigned by the Quality Lead or Production Quality Engineer.

Position Requirements

• High School Diploma or GED with minimum of 2 years’ experience in the quality system of the Mannford facility (or equivalency).
• Good communication skills and ability to explain and demonstrate technical methodologies to all levels of the organization.
• Highly motivated and ability to multi-task and prioritize on a daily basis.
• Ability to lead applicable Production personnel by example.