Job Title:  Quality Engineer

Job Summary

Responsible for meeting customer requirements for the manufacturing of surgicalinstruments and implants or instrument delivery systems from receiving raw material to the shipping of finished goods. Supports and enforces the development of internal systems and procedures to meet ISO standards and FDA quality systemregulations. Develops and implements inspection/validationtechniques necessary to verify products meet requirements at earliest point inthe production process.Specifies and implements new inspection equipment and instructs others inits proper use. Supports and implements systems in the areas of SPC, advanced quality, and design/development.

Duties and Responsibilities

• Assists in the development and implementation of systems and processes that foster continuous improvement for product development and/ormanufacturing.
• Responsible for ensuring cell processes are correctly base-lined & controlled. Knownvariabilityis to be accounted for through selection & frequency of inspection, sampling plans, or implementation of SPC.
• Completes the implementation and performance of gage R&R, process capability studies, design of experiments, and summaries as required to improve quality and to provide required deliverables to customers.
• Ensures processes released withuse of SPC where applicable and/or promote the utilization of SPC.
• Provides SPC & ongoing monitoring of SPC.
• Investigates deviations, OOS, complaints, returns, recalls, and field alerts.
• Supports the Material Review Board (MRB) for internal non-conformances and customer returns.
• Maylead or verify effectiveness of corrective and preventive actions (CAPAs).
• Mayliaise directly with customer representatives.
• Supervise and trainpersonnel inthe inspection of raw materials, in-process and finished goods byusing statistical sampling techniques and precisionmeasuring instruments to check conformance to requirements.
• Verify that all productionprocedures have been followed and the records such as Device Master Records and Device History Records are maintained per FDA & customer requirements and Paragon Medicalrequirements.
• Design inspection/validation steps to be takenbyoperations at the point of manufacture and integrate these steps into the manufacturing instructions.
• Responsible to create, implement and improve quality systems and procedures for meeting ISO 13485, FDA and customer quality systemrequirements.
• Work in conjunction with Cell Leaders to ensure CNC Machinists are knowledgeable and competent inthe use and care of sensitive measuring equipment and related requirements such as calibration, recording of data, expected variability, etc.
• Provide day-to-day oversight of quality including batch testing, inspection, calibration, environmental monitoring, qualification, document review, etc.
• Creates and supports ECN's and SCR's (product).
• Mayauthorize, initiate and/or approve product and process changes.
• Supports both internal and external audits of all corporate quality systems and demonstrates compliance through objective evidence.