Principal Process Engineer

TL;DR

Principal Process Engineer (Manufacturing): Provide technical and sustaining engineering support in a manufacturing area, recommending and implementing equipment and process modifications to meet quality standards and improve production efficiencies, yields, and manufacturing techniques. Focus on integrating equipment/material capabilities to meet process and technology specifications, developing manufacturing processes using statistical process control, and ensuring compliance with regulations in a regulated environment.

Location: Salt Lake City, Utah, United States of America (On-site)

Salary: $128,800.00 - $193,200.00 (USD)

Company

hirify.global is a global healthcare technology company developing solutions to alleviate pain, restore health, and extend life.

What you will do

• Provide technical and sustaining engineering support in a manufacturing area.
• Recommend and implement equipment and process modifications to improve quality, production efficiencies, manufacturing techniques, and production yields.
• Integrate equipment and material capabilities to meet process module and technology target specifications.
• Review product development requirements for compatibility with processing methods, including cost and schedule impacts.
• Lead innovation, development, and optimization of new manufacturing concepts, processes, and procedures for transfer to manufacturing operations (including feasibility, material/equipment selection, tooling/fixture installation, and input/output assessment).
• Develop manufacturing processes applicable to statistical process control, including measurement systems, and ensure processes and procedures comply with regulations.

Requirements

• Bachelor’s degree (Baccalaureate).
• Minimum 7 years of relevant experience, or Master’s with minimum 5 years relevant experience, or PhD with 3 years relevant experience.
• U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above.
• For degrees earned outside the United States, provide a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A).

Nice to have

• Deep medical device experience, preferably in vascular or neurovascular products.
• Proven expertise leading process development and scale-up activities in regulated environments.
• Recognized expertise in process validation, including owning a validation strategy and execution, with strong ISO 13485 knowledge.
• Advanced expertise in DFM and manufacturing methods (plastics, metals, specialized processes) and ability to drive cross-functional decisions.

Culture & Benefits

• On-site role with a minimum of 4 days per week onsite.
• Eligible for a short-term incentive called the hirify.global Incentive Plan (MIP).
• Benefits for regular employees working 20+ hours/week include health, dental, vision, HSA, healthcare FSA, life insurance, long-term disability, dependent daycare spending account, and tuition assistance/reimbursement.
• Additional benefits for all regular employees include 401(k) with employer contribution and match, paid time off, paid holidays, employee stock purchase plan, and employee assistance program.

Hiring process

• Application review followed by interviews to assess experience in process engineering and regulated manufacturing.
• Evaluation of fit for Principal-level responsibilities and U.S. work authorization requirements.