Careers that change lives
In this exciting role as a quality engineer you will have responsibility for maintaining existing supplier quality agreements by generating quality agreement amendments and addendaIn addition, you will have responsibility for completing 36 month periodic reviews of existing supplier quality agreements to determine if updates are required.
Our global quality strategy is rooted in the medtronic mission and our quality policyBeing a `trusted partner` means always putting patient safety first, upholding product quality, and maintaining the highest ethical standards in our business relationships and programs.
A day in the life
Maintain existing supplier quality agreements by generating supplier quality agreements amendments, addenda or new quality agreements with key suppliers including processing through cross functional approval at medtronic, including legal, quality and sourcing
Review and provide feedback on new supplier quality agreements that are drafted by pre-market and post-market supplier quality
Document the 36 month periodic review of supplier quality agreements and determine actions needed which include quality agreement amendments, addenda or new quality agreements
Initiation, review and/or approve supplier quality agreement data changes (dchs) and record changes (rchs)
Respond to questions and request that are sent to the group mailbox
Must have: minimum requirements
Bachelor’s degree in engineering, science or technical field with 2+ years of work experience in engineering and/or quality or advanced degree in engineering, science or technical field with 0+ years of work experience in engineering and/or quality
Nice to have
Experience working in medical device or other highly regulated industry preferred
Oral, presentation and written communication skills
Work in a team/partnership environment
Computer skills (microsoft- word, excel, powerpoint)
Solid understanding of technical principles i.e., supplier audits, corrective/preventive action and control plans
Knowledge of applicable gmp, fda and iso regulations
Together, we can change healthcare worldwideAt medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend lifeWe challenge ourselves and each other to make tomorrow better than yesterdayIt is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our teamLet’s work together to address universal healthcare needs and improve patients’ livesHelp us shape the future.
Physical job requirements
The physical demands described within the responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this jobReasonable accommodations may be made to enable individuals with disabilities to perform the essential functionsFor office roles: while performing the duties of this job, the employee is regularly required to be independently mobileThe employee is also required to interact with a computer, and communicate with peers and co-workersContact your manager or local hr to understand the work conditions and physical requirements that may be specific to each role(ada-united states of america)