Quality Engineer

Overview

The 3D Systems facility in Littleton, Colorado seeks an entry-level Quality Engineer to support excellence in the additive manufacturing of medical devices under the guidance of our Production Quality Manager. This vital role will learn and apply quality assurance principles across production and post-production processes for our state-of-the-art 3D printed medical solutions. The successful candidate will assist in implementing and maintaining rigorous quality systems that meet regulatory requirements while contributing to improvements in our manufacturing workflows.

Join our innovative team where you will develop your skills and directly impact patient outcomes by helping ensure our life-changing medical devices consistently exceed quality expectations!

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

• Quality Management System Support: Support execution, maintenance, and improvement of Quality Management Systems in accordance with USFDA CFR 820, ISO 13485, and AS9100 requirements.
• Technical Issue Resolution: Participate in complaint, CAPA, and NCR investigations, gathering product conformity information and coordinating with stakeholders to optimize quality while remediating processes, updating work instructions, and minimizing scrap.
• Product Quality Process Development: Utilize existing processes and inspection methods while developing new capabilities to meet technical requirements, including specifying, financially justifying, developing, and implementing new quality assurance methods.
• Process and Product Validation: Participate in cross-functional teams to develop and execute test protocols for verification and validation of updated products, materials, equipment, software, and processes, performing statistical analysis to assess design and manufacturing viability.
• Measurement System Analysis: Identify and evaluate measurement systems to ensure accuracy, precision, and stability in product conformity assessments.
• Analytics and Data Gathering: Strong aptitude for data analytics and data gathering preferred.

Education

• Bachelor's degree in Engineering or related technical field required.

Experience

• Relevant experience in regulated cGMP environments such as medical device manufacturing or pharmaceuticals required.

Knowledge, Skills & Abilities

• Foundational understanding of quality assurance and reliability principles in product development and/or manufacturing operations.
• Basic knowledge of cGMP requirements, ISO 13485 Quality Management Systems, and/or AS9100 standards.
• Technical aptitude with ability to learn and interpret specifications across diverse products and materials.
• Analytical thinking skills with eagerness to support and improve engineering processes for advanced technology implementations.
• Ability to create clear technical documentation and reports with attention to detail.

Applications accepted online through February 20th, 2026

#LI-MP1

3D Systems is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, ethnicity, religion, sex, age, sexual orientation, genetic information, marital status, gender identity or national origin or because he or she is an individual with a disability or a disabled veteran, Armed Forces service medal veteran. The Company also provides applicants with equal employment opportunities without regard to pregnancy, childbirth, medical needs arising from pregnancy or childbirth, and related medical conditions including, but not limited to, lactation.

Primary Location
: US-CO-Littleton

Work Locations
: USA-CO-Littleton

80127

Job Level
:
Individual Contributor

Travel
:
No

Type of Position
:
Employee

Job Posting
:
Feb 6, 2026, 6:06:47 PM