Job Summary

We are seeking a highly skilled and experienced Quality Engineer III to support our manufacturing operations. This role focuses on defining, implementing, and continuously improving quality practices. The ideal candidate will have expertise in technical guidance and measurement methodologies, ensuring high standards for precision components and assemblies in the medical device industry.

Key Responsibilities

• Provide quality engineering support for manufacturing processes and project management initiatives.
• Develop inspection requirements, facilitate PFMEAs, resolve discrepant material issues, and maintain quality documentation, including control plans and inspection plans.
• Analyze manufacturing data to identify improvement opportunities and implement corrective actions.
• Serve as the quality interface for production teams and respond to customer complaints through failure analysis, corrective and preventive actions, and trend analysis.
• Conduct internal audits, manage audit findings, generate reports, and determine appropriate corrective and preventive actions.
• Coach and mentor Quality Engineers at levels I and II.
• Act as a subject matter expert in one or more areas of the ASQ Quality Engineer Body of Knowledge.
• Lead and participate in significant company projects, providing expert quality recommendations.
• Support Quality Inspectors in ensuring inspection plans align with customer product requirements.
• Assist with the validation of processes, equipment, and metrology.
• Create validation protocols and analyze associated data.
• Ensure the proper implementation, maintenance, and functioning of business systems.
• Support and comply with the company Quality System, ISO standards, and medical device regulations.
• Partner with teams across sales, marketing, customer service, engineering, quality, and finance.
• Understand customer needs and the core business markets served.

Qualifications

Education

• Bachelor’s degree in mechanical, industrial, or another engineering discipline.

Experience

• Experience operating and providing training on a variety of inspection equipment.
• Experience in a machining or manufacturing setting.
• Knowledge of quality systems, regulatory requirements, and industry standards.

Skills

• Advanced knowledge of blueprint reading and GD&T.
• Statistical expertise in DOE and capability studies.
• Proficiency in Minitab.
• Process management experience.
• Experience with ERP and quality systems.
• Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint, and Publisher).
• Clear and effective verbal and written communication skills.
• Strong attention to detail and organizational skills.
• Ability to work effectively in a fast-paced team environment.
• Ability to prioritize and multitask.

Personal Attributes

• Proven ability to consistently achieve short- and long-term business results.

Benefits

• Competitive wages and a comprehensive benefits package.
• Opportunities for professional growth and development.
• A positive, collaborative work environment focused on continuous improvement.
• An opportunity to contribute to a company that plays a vital role in the medical device industry.

How to Apply

Interested candidates are encouraged to click the “Apply Now” button to submit an application.