A company is looking for a Development Quality Engineer.
Key Responsibilities
Provide design quality engineering support to new product development teams, ensuring compliance with regulations and quality standards
Lead and support the completion of design control deliverables, verification and validation testing, and documentation for U.S. and EU market submissions
Manage risk activities, develop and validate test methods, review quality documentation, and collaborate with cross-functional partners throughout the product lifecycle
Required Qualifications
Bachelor's Degree in Engineering or a Technical Field is required
5+ years of engineering experience in quality, design verification, and / or product development is required
Experience in the medical device industry with knowledge of design control and regulatory standards (ISO 13485, ISO 14971) is required
Experience in test method development, validation, and risk documentation (FMEA, risk assessments) is required
Experience with electro-mechanical or implantable devices is preferred
Quality Engineer • Lexington, Kentucky, United States