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Quality Engineer
2 months ago
Our recruiting philosophy is centered on attracting talented individuals committed to delivering innovation. Rooted in a talent dense culture that fosters continuous growth and achievement, both personal and organizationally, we've been organically scaling at a rapid pace and have aggressive hiring plans for the years ahead. By joining Lexington Medical, you will have the opportunity to impact the lives of millions of patients worldwide and thrive in a growing company.
As a Quality Engineer at Lexington Medical, you will drive the quality system and design assurance activities and play a key role in creating a world-class quality management system and building a quality function that is core to the company's success.
What you will do:
- Drive Design Assurance activities throughout the Product Life Cycle
- Provide expertise in Risk Management, Design Verification and Validation, Statistical Methods and Design Controls
- Define and implement processes within the Quality Management System
- Drive quality system execution to US and international standards, including development of quality and risk management plans
- Drive continuous improvement projects, and proactively identify and implement best-in-class quality engineering practices
- Develop test methods and inspection procedures and implement process control systems to support the development, qualification, and on-going manufacturing of products
- Support supplier quality management, including conducting sub-contractors and component supplier audits
- Apply systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues
- Bachelor's or Master's degree in Biomedical Engineering, Mechanical Engineering, or related field
- 2+ years of experience in design quality engineering, in the medical device industry (experience with electrical equipment is a plus)
- Experience developing and implementing processes within quality management systems.
- Experience in new product development and introduction (NPD/NPI), and in design transfer
- Strong working knowledge of US and international medical device regulations and standards, including 21 CFR 820, EU 2017/45 (MRD), ISO 13485, ISO 14971, IEC 60601, and IEC 62366
- Demonstrated knowledge of design controls, process validation, risk management, and change control
- Demonstrated application of systematic problem-solving techniques and defect avoidance methodologies
- Experience participating in material review boards
- Supplier quality experience is a plus
- Strong team orientation and ability to lead in a cross-functional environment
