Process Development Engineer II

Medtronic • Danvers, MA

2d • Onsite

About The Position

We anticipate the application window for this opening will close on - 13 Apr 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 Process development engineer in the AME organization As a Process Development Engineer II within the Advanced Manufacturing Engineering (AME) team in Danvers, MA, you will play a key role in developing and optimizing manufacturing processes that enable the successful launch and scalable production of life-saving medical technologies. In this role, you will collaborate cross-functionally with Product Development, Quality, Manufacturing, and Operations teams to design and implement robust manufacturing processes that meet performance, quality, and regulatory requirements. You will contribute to both new product development initiatives and continuous improvement efforts for existing products, helping bring innovative medical technologies from concept to commercial production. This is an exciting opportunity to work in a fast-paced, innovation-driven environment where engineering expertise directly impacts patient outcomes around the world. 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’re working a fully onsite schedule, with the expectation of a full 5-days a week being onsite, as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.

Requirements

• Bachelors degree and minimum of 2 years of relevant experience OR Masters degree with a minimum of 0 years relevant experience
• 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

• Degree in Mechanical Engineering, Manufacturing Engineering, Chemical Engineering, Biomedical Engineering, or similar field
• Experience supporting manufacturing process development or process engineering
• Experience with new product development (NPD) or product transfer to manufacturing
• Familiarity with statistical process control (SPC), process capability analysis, and data-driven problem solving
• Experience working with automation, manufacturing equipment, tooling, or fixture design
• Knowledge of medical device manufacturing, regulated environments, or FDA/ISO quality systems
• Experience collaborating with cross-functional teams including R&D, Quality, and Operations
• Familiarity with Lean manufacturing or continuous improvement methodologies

Responsibilities

• Provide technical and sustaining engineering support for manufacturing operations and process development initiatives.
• Lead or support the development, optimization, and implementation of manufacturing processes for new and existing products.
• Recommend and implement equipment, tooling, and process modifications to improve product quality, production efficiency, and manufacturing yields.
• Evaluate and integrate equipment and material capabilities to achieve process module and technology target specifications.
• Collaborate with product design and development teams to ensure manufacturing processes and product designs are compatible and scalable.
• Participate in process feasibility studies, technology scouting, and concept development to identify innovative manufacturing approaches.
• Support material selection, equipment selection, tooling/fixture design, and equipment installation during process development activities.
• Develop and apply statistical analysis and data-driven methods to evaluate process performance and support decision making.
• Design manufacturing processes compatible with statistical process control (SPC) and measurement systems.
• Document engineering work, including process development reports, validation documentation, and standard work instructions.
• Partner with cross-functional teams to ensure processes comply with quality system requirements and applicable regulatory standards.
• Support the transfer of developed processes into manufacturing operations, ensuring robust and scalable production readiness.

Benefits

• Medtronic offers a competitive Salary and flexible Benefits Package
• 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)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level