Serves as the Management Representative to monitor and report on the adequacy, effectiveness
and continuing suitability of the company's Quality Management System (QMS) in accordance
with ISO 13485:2016, established policies/procedures, and applicable regulatory requirements.
Promote awareness of applicable, new and/or updated in-vitro diagnostic medical device
regulations and standards.
Manage the document control, engineering change control, and records control process including
external origin documents.
Evaluate, monitor, and re-evaluate suppliers. Maintain the Approved Supplier List (ASL).
Manage the internal audit program to ensure timely execution in accordance with published
schedule.
Manage the calibration program to ensure all monitoring and measuring equipment are inducted,
calibrated, reviewed, and monitored in a timely manner.
Participate in design control, risk management, and software development activities throughout
the lifecycle(s) of medical devices at BioCheetah. Participate in risk assessment (FMEAs and SHA)
and risk control activities of device design, use, and manufacturing.
Participate in the validation of analytical test methods, process validations, and computer
software used in the quality management system, production, and monitoring/testing.
Participate in the handling of non-conforming products including but not limited to investigation,
corrective/preventive actions, and disposition of affected products.
Participate in the preparation of premarket regulatory submissions for commercial distribution.
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