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Engineering Tech V - CNC Programming

Medtronic
United Statesfull_timeVerifiedPosted 24 Sept 2025
💰 $123,000/yr

About the role

We anticipate the application window for this opening will close on - 27 Sep 2025


 

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

People-centered, data-driven, connected. We're solving the world's biggest health challenges with healthcare technology. We fuse technology and research for groundbreaking solutions. From less-invasive surgery that minimizes a patient's downtime to the world’s smallest pacemaker, our technology transforms lives. At Medtronic, at our Warsaw production facility, also known as Warsaw Orthopedics, manufactures Spinal Implants and Brain/ENT components.

Responsibilities may include the following and other duties may be assigned.

  • Responsible for the development of all CNC machining program code.
  • Review engineering drawings and initiates changes, or recommendations, for manufacturing tools, fixtures, CNC programs, through the change control system.
  • Provides technical support to engineers to achieve improvements in cycle-time, yield, unit cost, quality, safety and compliance of production and operations processes and products.
  • Monitors instruments and equipment and collects operating data, including calibration, inspection, testing and repair activities, to assist in making on-line adjustments to instruments, equipment, or products.
  • Analyzes and resolves malfunctions and deviations of instruments and control systems to identify and resolve problems.
  • Conducts, analyses and prepares reports using metrics from salvage tracking, trending, reporting and root-cause analyses.
  • Maintains process designs to optimize process, equipment and facility use while conforming to standard operating procedures (SOPs) and Good Manufacturing Practices (GMPs).
  • Completes activities of the change control policy and Corrective and Preventive Action (CAPA) system in accordance with policy.
  • Work in cross-collaborative teams to execute risk management activities (i.e. pFMEA)
  • Creates conceptual designs for new fixtures and special cutting tools. Which can require tool design reviews with Tooling Team personnel, purchasing personnel and outside tool suppliers.
  • May make recommendations to leadership on plant layout.
  • May in determining appropriate machine platforms for product and review any necessary capital equipment requirements along with specifying required capital tool holders.
  • Develops manufacturing setup sheets for all machining operations for new products.
  • May recommend equipment acquisitions. Works with equipment suppliers on equipment specifications, quoting of specified equipment and delivery schedules.
  • Reviews product drawings for manufacturability. Initiates drawing changes with the product design engineer to improve manufacturing quality and reduce costs.
  • Proactively execute and support development of validation and qualification studies. Provide input to assist in developing the strategy with appropriate teams.
  • Support product launches, transfer of product and core business initiatives
  • May lead in the training of new team members as well as training for new CNC machine programs, machining processes, or machining equipment.
  • Travel as required for company business needs.

Preferred Qualifications

  • Experience with CAM/CAD software: Mastercam , Pro/E and Vericut
  • Direct experience with providing direct machining support such as creating new programs, troubleshooting and/or updating existing programs.
  • Advanced level of understanding machines platforms such as mills, chucker and Swiss style lathes.
  • Proven experience troubleshooting machining issues, research and developing tools, fixtures and programming solutions to solve quality and safety issues.
  • Working knowledge of industry standards and regulatory requirements. (Including, but not limited to: ISO 13485, ISO 14971, MDD 93/42 EEC, PAL, CMDR, and 21 CFR Part 820)
  • Understands impact of compliance to the requirements and how it relates to their job, or is aware of resources available to them to assist with determining impact.
  • Strong oral and written communication skills.
  • Good interpersonal skills.
  • Ability to work in a fast paced environment.
  • Ability to work well under pressure and maintain a positive, and enthusiastic attitude.
  • Eagerness to learn and expand responsibilities.
  • Ability to work effectively in a team environment and build strong working relationships.
  • Willingness to participate in continuous improvement initiatives.

Required Knowledge and Experience:

  • Requ

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Company

Medtronic

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