Quality Engineer - Medical Device
Greene Group Industries
Port Huron
Join our team as a Quality Engineer where you can make a significant impact on product excellence while growing your career in a dynamic environment focused on innovation and continuous improvement!
Responsibilities
- Provide direct, on-the-floor support to manufacturing operations.
- Analyze production data and identify areas for improvement in real-time to optimize manufacturing processes and minimize downtime.
- Utilize ANSI sampling, AQL, problem solving techniques to determine product acceptance, evaluate process capabilities CPK and determine product and continuous improvement plans.
- Generate internal quality documentation such as advance process quality planning APQP, SOPs and work instructions and submitting First article inspection report FAIR/ production planning approval process for customer approval.
- Review nonconforming materials for disposition, participate in and / or lead quality review meetings.
- Perform part inspections on metrology equipment such as calipers, micrometers, gauge pins, and Keyence for dimensional inspection to meet product specification.
- Work with Engineering to review designs for measurement fixtures and plans for new product launches.
- Ability to be active part of Investigations, support the team by following up on CAPAs status and be a guidance to the business partners.
- Analyze performance reports and process control statistics; investigate and analyze relevant variables affecting products and processes.
- Perform and analyze Gage R&R and measurement systems analyses.
- Support GGI’s quality management system auditing activities and compliance of Quality Management Systems. Participate in internal audits and Fresh Eyes Audits for the Greene Group Business Units.
