Quality Engineer II
Becton Dickinson · Covington BMD
The apply link worked recently (not employer-confirmed).
Role summary
Quality Engineer II supports product development and design changes while ensuring regulatory compliance and product quality at this medical technology company. The role involves serving as a quality representative on cross-functional teams, managing Design Controls and validation activities, and maintaining quality system documentation throughout the product lifecycle. The ideal candidate has FDA-regulated industry experience and expertise in quality systems, risk management, and design principles.
What they're looking for
- Bachelor's degree in Engineering, Engineering Technology, Science, or related technical field
- Minimum 3 years experience in FDA-regulated industry
- Working knowledge of Design Controls, validation principles, and risk management
- Experience creating, reviewing, and maintaining technical and quality documentation
- Strong written and verbal communication skills for cross-functional collaboration
- Knowledge of Quality Management Systems and regulatory requirements
- Experience writing and executing validation protocols for processes, software, or products
What you'll be doing
- Serve as Quality representative on product development and process change project teams
- Create, review, and maintain Design History Files and quality system documentation
- Develop and review validation protocols, risk assessments, and compliance documentation
- Support Design Control application, design transfer, and product lifecycle activities
- Participate in internal and supplier audits to ensure Quality Management System compliance
Privacy & handoff
This role links to Becton Dickinson's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.