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.
Summary
The Global Quality Management Systems Manager will implement and drive maintenance of quality system requirements, including document management, audits, CAPA, quality metrics reporting, management review, and training.
Global Activities:
Bedford Site-Level Activities:
Required Experience, Education, Skills, Training and Competencies
Travel Requirements
Physical Requirements
Novanta is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy.
Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process.
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Join Novanta as a Manager of Global Quality Management Systems in Bedford, MA, and power your career with innovations that truly matter! Our cutting-edge technologies are designed to transform healthcare and advanced manufacturing, enhancing productivity and redefining what's possible. As part of the global Novanta team, you will be instrumental in implementing and maintaining quality system requirements that drive excellence across various mission-critical applications, including minimally invasive surgeries and robotics. You'll be responsible for building strong relationships with stakeholders, overseeing regulatory and internal audits, and managing corrective and preventative actions. Your day-to-day activities will involve facilitating quality operational reviews, managing site-level auditing requirements to adhere to ISO standards, and contributing to a culture that values teamwork and empowerment. With a collaborative spirit, you will ensure our Global Quality Management System evolves into an Integrated Management System. If you're ready for a challenging role that requires both strategic oversight and a detail-oriented approach, join us at Novanta where your expertise will help shape the future of technology in critical sectors.
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Novanta is a trusted technology partner to medical and advanced industrial OEMs (original equipment manufacturers), with deep proprietary expertise in precision medicine and manufacturing, medical solutions, and robotics and automation. We enginee...
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