Quality Assurance Engineer

Job Details:

Job Location:

Grove City OH - Grove City, OH 43123, Position Type:
Full Time, Education Level: Associate's Degree, Travel Percentage:
None, Job Shift: Standard Business Hours, Job Category:
Biotech, Tosoh Bioscience, Inc., based in South San Francisco, CA is a U.S. subsidiary of Tosoh Corporation's Bioscience Division, headquartered in Tokyo, Japan. Established in the United States in 1989, Tosoh Bioscience has become known throughout the Americas for providing sophisticated diagnostic systems to doctor’s offices, hospitals and reference laboratories. Tosoh remains at the forefront with a world class network of research facilities, scientists, engineers and customer support specialists.

Under the direction of the Quality Assurance Manager, the Quality Assurance Engineer performs critical Tosoh Bioscience Inc. (TBI) functions in support of TBI’s Quality System in compliance with FDA Code of Federal Regulations (21 CFR 820), ISO 13485, ISO 14971, and Tosoh Bioscience Quality Policies and Procedures. The Quality Engineer assists in the implementation, management and continuous improvement of the TBI Quality System and provides cross-functional engineering support to Operations, Facilities Control and Manufacturing Project teams through system validations and data monitoring.

The Quality Assurance Engineer will report to the Quality Assurance Manager.

• Assists scientific staff in identifying and documenting requirements for new instruments, medical devices, and equipment to ensure that each meets required specifications.
• Generates Risk Management Assessment reports for Equipment and Engineering Plans along with SME.
• Prepares protocols for installation, operational and performance qualification of instruments, performs and/or directs the execution of these protocols and completes the final validation reports.
• Performs quality testing on devices to determine engineering tolerances and validation schemes.
• Performs and documents all routine calibration and maintenance of applicable equipment.
• Assists in the development of the TBI Master Validation Plan with SME.
• Writes Quality System procedures for instrument operation, routine maintenance and calibration.
• Coordinates instrument maintenance and calibration performed by external vendors.
• Manages the TBI environmental control monitoring system, and coordinates responses and corrective actions and preventative actions to alarms and out-of-specification conditions.
• Responds to equipment malfunctions and coordinates repairs performed by external vendors.
• Trains TBI employees in the operation of new laboratory equipment and response to environmental monitoring system alarms.
• Maintains detailed equipment records on the purchase, qualification, calibration, repair and maintenance in compliance with documented Quality System procedures.
• Assists in internal audits to assess TBI compliance with Quality System policies and procedures as needed.
• Assists in the development and monitoring of quality metrics.

An Associate's or Bachelor’s Degree is preferred in a technical discipline such as biomedical sciences engineering, engineering, or a related field and/or equivalent experience.

• Minimum of five years of relevant facilities and/or manufacturing IVD industry experience in an FDA-regulated or ISO
  13485 environment with exposure to cGMP practices.
• Ability to understand Contract Manufacturing versus Manufacturer of Record quality and regulatory cGMP requirements for Facilities, Operations, and Manufacturing of Clinical Chemistry IVDD.
• Organizational, planning and detailed follow-up skills required. Ability to utilize tasking, scheduling, and other project management…