Job Description
Basic Purpose of Position: Assist in the development and implementation of Quality Procedures in compliance with the ISO-13485 Standard.
Primary or Major Responsibilities:
- Failure mode and root cause analysis of incoming, production and field failures
- Production process review and auditing
- Assist in internal and supplier audits
- Create quality plans
- Create Part Quality Plans in accordance with customer requirements
- Maintain regulatory compliance
- Maintain Device History Files
- Support the development, maintenance, and auditing of the Quality Management system.
- Assist in development and implementation of applicable processes to meet Customer requirements, including training, problem solving, and review meetings.
- Manage trace matrix for medical device design control
- Lead project risk management activities
- Work directly with customers to develop product level and system level design specifications
- Support FDA submission with project documentation
- Compile CE technical files
- Drive continuous improvement across facility Key Process Indicators.
- Aid in reliability testing.
Safety:
- Ensure that all assignments are performed in compliance with all applicable Federal, State, Provincial and Company safety and health regulations, and where applicable, proper personal protective equipment is utilized.
Minimum Requirements:
- Bachelor's degree in Engineering field or area of study deemed acceptable by the hiring team.
- Minimum of 3 to 5 years engineering experience in related manufacturing position.
- Experience developing medical product requirements and specifications
- Experience developing and executing verification protocols for medical devices
- Thorough understanding of FDA medical device regulations and design control processes
- Thorough understanding of ID regulatory requirements
- Thorough understanding of IEC 60601 3rd edition
- Ability to function effectively in a team environment.
- Effective communication skills driven by attention to detail.
- Strong DFM and NPI skills.
- Excellent analytical skills using Six Sigma and Lean Principles.
- Good working knowledge of quality/reliability engineering statistical techniques.
- Self- motivated and self- managed.
- Ability to handle multiple projects at the same time.
Strongsville, OH
22740 Lunn RoadStrongsville, OH 44149
440-878-4630
As an equal opportunity employer, Sparton Electronics is committed to a diverse workforce. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact Kelly Stewart for assistance.
EOE M/F/V/D

