Engineering Manager

Medtronic•Mounds View, MN

45d•Onsite

About The Position

We anticipate the application window for this opening will close on - 31 Mar 2026 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Medtronic is seeking a new Engineering Manager within the post-market reliability team supporting the Cardiac Rhythm Management group. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We are working onsite a minimum of 4 days per week as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. This role will require less than 10% of travel to enhance collaboration and ensure successful completion of projects.

Requirements

Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A) AND minimum of 5 years relevant experience, OR advanced degree with a minimum of 3 years prior relevant experience
Experience leading complex projects/programs
Experience with Design Control, Change Development processes, and CAPA
Experience creating and maintaining Risk Management Files to the latest ISO 14971 standards
Strong working knowledge of Quality System Regulations such as (QSR 21 CFR 820), ISO 13485, ISO14971 and other medical device associated regulations
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required

Nice To Haves

Experience leading or managing a team of Quality Professionals
Familiar with implantable medical devices and product specific industry standards.
Experience auditing the FDA Quality System Regulation, ISO 13485, and the Medical Device Directive
Experience with CAPA and/or root cause failure analysis
Green Belt Six Sigma/DRM Training/Certification
Demonstrated working knowledge of process validation, statistical methods, risk management
Experience with Product / Packaging Stability, Biocompatibility, Sterilization, Ship Testing, HALT/HASS

Responsibilities

Manage a team of reliability engineers supporting post-market surveillance and risk management activities including complaint investigation, complaint monitoring, health hazard evaluations, CAPA, product containment and field corrective actions
Quality management representative for products within the cardiac pacing therapies and cardiac diagnostics & services portfolios
Maintain deep familiarity and execute activities in accordance with FDA 21 CFR Part 820, ISO 13485, ISO14971 and other medical device associated regulations; support external inspections on an as needed basis
Partner closely with R&D and Quality colleagues to embed best practices in technical rigor, simplify execution, and bring forward individual perspectives that strengthen decision-making and solution design

Benefits

Medtronic offers a competitive Salary and flexible Benefits Package
We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Health, Dental and vision insurance
Health Savings Account
Healthcare Flexible Spending Account
Life insurance
Long-term disability leave
Dependent daycare spending account
Tuition assistance/reimbursement
Simple Steps (global well-being program)
Incentive plans
401(k) plan plus employer contribution and match
Short-term disability
Paid time off
Paid holidays
Employee Stock Purchase Plan
Employee Assistance Program
Non-qualified Retirement Plan Supplement (subject to IRS earning minimums)
Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums)