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.
Essential Functions:
Support, maintain, and improve QMS to ISO 13485 and 9001 standards
Conduct supplier QMS audits and support 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
Job Qualifications:
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
Required Education:
Bachelor’s Degree in Engineering or related discipline
Required Experience:
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
The salary for this role will range from $69,075 to $100,000 annually based on full-time employment. Salary offers are based on a wide range of factors including but not limited to location, relevant skills, training, experience, education, etc. Certain roles may be eligible for performance-based incentive compensation and/or long-term incentives. Incentives could be discretionary or non-discretionary depending on the plan. Novanta supports all aspects of your life's needs. This position provides a full range of medical, financial, and other aspects to make your quality of life better.
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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