Quality Engineer
About The Position
Build a career powered by innovations that matter! At Novanta, our innovations power technology products that are transforming healthcare and advanced manufacturing—improving productivity, enhancing people’s lives and redefining what’s possible. We create for our global customers engineered components and sub-systems that deliver extreme precision and performance for a range of mission-critical applications—from minimally invasive surgery to robotics to 3D metal printing. Novanta is one global team with over 26 offices located in The Americas, Europe and Asia-Pacific. Looking for a great place to work? You have found it with a culture that embraces teamwork, collaboration and empowerment. Come explore Novanta. In this exciting and challenging role you will work for Cambridge Technology, Inc. Cambridge Technology (CTI) is a global leader in galvanometer-based scanning technology and associated mirrors. These products are used in various laser-based applications including medical devices, rapid prototyping, converting, marking, and coding and many more. Cambridge Technology’s products deliver up to 1 micron accuracy and marking speeds of over 1,000 characters per second.
Requirements
- Comprehensive root-cause investigation experience and solid understanding of corrective and preventive action processes including the applicable tools and techniques.
- Must be detail-oriented, be able to accurately prepare statistical reports and technical documents in support of company objectives .
- Must have proven leadership experience coordinating company cross-functional team members and external supplier representatives.
- Excellent critical thinking and problem-solving skills
- Detail-oriented problem solver who is schedule-orientated
- Ability to work independently, as part of a larger cross-functional team and/or lead cross-functional teams comprised of Cambridge Technology colleagues and supplier representatives
- Bachelor’s Degree in Engineering or related discipline
- 5 + years of related experience in Quality or related field
- Working knowledge of ISO 13485
- Working knowledge of risk management processes
- Strong leadership and communication skills
Responsibilities
- Support, maintain , and improve QMS to ISO 13485 and 9001 standards
- Conduct supplier QMS audits and s upport internal and external QMS audits
- Develop and manage supplier qualification and management program
- Manage FAI process
- Develop and manage MRB, SCAR, CAPA processes
- Generate, review , and approve Engineering Change Orders
- Develop test methods and inspection procedures and implement process control systems to support the development, qualification, and on-going manufacturing of products
- Use data to drive process improvements
- Design and implement computer-based quality system processes , including development of training
Benefits
- This position provides a full range of medical, financial, and other aspects to make your quality of life better.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
