A Day in the Life
- Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product
- Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment
- Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
- Participates in corrective/preventive action teams in resolving production and customer issues. Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
- Performs or provides guidance to Manufacturing Engineering on effective Process Validation, Test Method Validation and nonconforming material investigations.
- Ensures that local quality records supporting finished devices such as Device Master Records, Device History Records, Master Validation Plans, Process FMECAs, etc.. are accurate, current, and compliant to regulations.
- Identifies and implements continuous improvement ideas based on observations during day-to-day activities
Minimum Qualifications:
- Currently pursuing a Bachelor's degree in Engineering or related technical field
- Must have current work authorization and be legally authorized to work in Canada. Medtronic Montreal does not provide work authorization sponsorship for intern positions.
- Participants must be able to participate full time (40 hours/week) from Monday to Friday
Preferred Qualifications:
- Minimum of a 3.0 out of 4.0 cumulative GPA
- Prior work on projects in a team environment
- Leadership experience in student groups, volunteer experience, and related extracurriculars
- Relevant academic project and/or internship experience
Physical Job Requirements Benefits \& Compensation
Medtronic
