Sr. Principal Mechanical Design Engineer (Medical Devices)

Location: Mounds View, Minnesota, United States; minimum of 4 days onsite, with work performed in R&D laboratories and manufacturing facilities and travel to suppliers and design or manufacturing sites as required.

Salary: $160,800–$241,200 per year in U.S. locations, excluding Puerto Rico and specific California locations.

Company

hirify.global develops healthcare technologies focused on alleviating pain, restoring health, and extending life, including electrophysiology therapy products.

What you will do

• Serve as the design owner for released product engineering teams, planning, developing, and executing testing and analysis during product change implementation.
• Design, develop, analyze, troubleshoot, and provide technical support during product development and manufacturing.
• Drive improvements in product performance and manufacturability, cost, quality, supply continuity, and preservation of design intent.
• Perform hands-on root-cause investigations on the manufacturing floor and design studies to identify process parameters and resolve technical issues.
• Define and perform verification and validation activities, support product improvements and pre-clinical studies, and evaluate existing technologies.
• Coordinate with program management, manufacturing, quality, suppliers, consultants, and cross-functional teams; document results in engineering reports and presentations and mentor junior engineers.

Requirements

• Bachelor’s degree with at least 10 years of relevant experience, or a master’s degree with at least 8 years of relevant experience, or a PhD with at least 6 years of relevant experience.
• Experience in complex mechanical system design and product risk management.
• Ability to collaborate with diverse cross-functional teams and interact professionally across organizational levels, including global, multi-site, and multi-business-unit stakeholders.
• Ability to apply statistical methods and science-based decisions to design experiments and implement improvements.
• Demonstrated ability to deliver quality technical work within project schedules and deadlines in a fast-paced, deadline-driven environment.
• For bachelor’s degrees earned outside the United States, the degree must satisfy the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A).

Nice to have

• Experience in the medical device industry and high-volume manufacturing.
• Experience with issue investigation and CAPAs.
• Experience in 3D modeling, finite element analysis, and statistical design analysis.
• Experience in process and test method development and validation.
• DRM Greenbelt certification or above.
• Hands-on mentality, excellent verbal and written communication, and strong interpersonal skills.

Culture & Benefits

• Full-time regular employment with health, dental, vision, life, disability, and retirement benefits.
• Health Savings Account, Healthcare Flexible Spending Account, dependent daycare spending account, and tuition assistance or reimbursement.
• Paid time off, paid holidays, paid sick time where applicable, and Employee Assistance Program.
• Incentive plans, 401(k) employer contribution and match, Employee Stock Purchase Plan, and other retirement programs.
• U.S. work authorization sponsorship is offered for Principal-level roles and above when specialized expertise aligns with long-term business needs.