Process Development Engineer Jobs in Denver, CO (NOW HIRING)

3D Systems Healthcare is seeking an innovative, results-driven Intermediate Product Development Engineer with expertise in modern product development methodologies to join our mission of Transforming Manufacturing for a better future! In this role, you will design cutting-edge medical devices utilizing state-of-the-art additive manufacturing processes, develop optimized end-to-end workflows and work instructions, and collaborate with multidisciplinary teams including surgeons and clinical partners to deliver products that meet technical, regulatory, and quality requirements on time and within budget. You will be at the forefront of emerging technologies and industry best practices while ensuring compliance with evolving regulatory guidance for medical devices and additive manufacturing. This is your opportunity to directly impact patient outcomes while working with breakthrough technology that is reshaping the future of healthcare!

This role has an onsite work schedule requiring the person to be in the onsite location 5 days a week.

• Competitive Compensation Package: $76,400 - $100,000 per year. Our employees are the best part of our company. We want you to feel valued, appreciated, and included. Because of this, we make sure your hard work is recognized.
• Paid Leave (US ONLY): Enjoy time away from work with Company paid holidays and a flexible working schedule through our paid time off (PTO) policy.We are a company that values you and makes sure you take time for yourself.
• 401(k): Prepare for a secure retirement with our 401k plan, which includes an employer matching contribution.
• Comprehensive Health & Wellness Plans: We offer a comprehensive benefit package that includes medical, dental and vision coverage, company-paid short-term and long-term disability insurance, as well as company-paid basic life insurance that supports you during your career with us. We believe that taking care of our employees is essential, and these benefits reflect our commitment to your health, security, and peace of mind.
• Global Team: With our state-of-the-art corporate headquarters in Rock Hill, South Carolina, our global team operates worldwide. Experience a workplace comprised of talented individuals who are passionate about serving our customers and each other.
• Innovative Culture: Innovation is at the heart of what we do! Since our founding in 1986 by Chuck Hull, the inventor of 3D printing, we have continuously pushed the boundaries of what is possible with additive manufacturing. When you join 3DS, you will have the opportunity to work with cutting edge technology in an innovative and collaborative culture!
• Connection & Engagement Opportunities: We strive to cultivate an environment where our diverse global workforce can connect and thrive. Our Employee Resource Group program, Employee Recognition program, and 3D Gives Back program are just a few examples of how you will be empowered to build connections, celebrate wins, and make a meaningful impact. 

As an Intermediate Product Development Engineer, you will collaborate with cross-functional project teams and contribute to innovation across the full product development cycle:

• "Deliver Extraordinary": Work directly with customers and surgeons to gather stakeholder input, translate clinical needs into design requirements, and provide our partners with the best service and solutions
• Lead and collaborate: Lead internal project teams and drive cross-functional collaboration to manage the development of patient-specific devices in adherence with Design Controls and Quality Management Systems
• Design and prototype: Generate and iterate device concepts using our advanced portfolio of metal alloy and polymer 3D printing technologies, from initial concept through final commercial product
• Establish processes: Create and document optimized workflows for customer interface, design, additive manufacture, and quality control for patient-specific medical devices
• Drive quality and efficiency: Develop robust process controls, drive verification and validation activities, and champion process improvement initiatives that enhance quality and consistency while reducing costs and timelines

Education:

• Bachelor's degree in Biomedical Engineering, Mechanical Engineering, or related technical discipline; or equivalent skills and work experience

Experience:

• 2 years of product development experience in a controlled industry
• Exceptional communication skills with design teams, stakeholders, and team members
• Proven ability to collaborate effectively with cross-functional teams
• Understanding of medical device design controls and regulatory pathways
• Experience establishing and executing verification and validation requirements
• Proficiency in additive manufacturing workflows and process controls
• Strong technical writing and written communication skills

Preferred Qualifications:

• Master's degree in Biomedical Engineering or Mechanical Engineering
• Experience with end-to-end development of patient-specific medical devices, particularly in plating/fixation and/or CMF/dental applications
• Advanced expertise in additive manufacturing workflows and process controls
• Solutions-driven mindset with ability to quickly learn, pivot, and innovate
• History working with clinical teams - acquiring input, translating feedback into actionable solutions, and leading cadaver labs
• Background in biocompatibility, design, quality control, statistics, or project management

Applications accepted online through July 24, 2026

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