Senior Supplier Quality Engineer

3D Systems is seeking a highly skilled and experienced Senior Supplier Quality Engineer to support our global operations in Littleton, Colorado and Leuven, Belgium, serving the medical device and aerospace industries. This role serves as a key quality leader responsible for supplier quality strategy, supplier development, risk management, and continuous improvement across the supply chain. The successful candidate will work independently to manage complex supplier quality challenges, drive supplier performance improvements, lead supplier quality initiatives, and ensure compliance with applicable regulatory and industry requirements. The ideal candidate is a proactive problem solver with strong supplier quality, auditing, and continuous improvement expertise who thrives in a fast-paced, regulated manufacturing environment. Join 3D Systems and help shape the future of additive manufacturing while contributing to innovative technologies that improve lives and transform industries around the world.

This position requires the individual to work onsite at the Littleton, Colorado facility five days per week.

• Competitive Compensation Package: $85,000 - $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.Yep, you read that correctly. 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 across more than 13 countries 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 3D, you will have the opportunity to work with cutting edge technology in an innovative and collaborative culture!
• Talent Development: At 3D Systems, we invest in talent programs to support employees with opportunities to grow, contribute, develop, and thrive in their careers.
• 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.

Travel

• This position requires approximately 25% domestic and international travel to supplier locations and company sites.

Supplier Evaluation and Qualification

• Lead qualification and approval of new suppliers, including critical and high-risk suppliers.
• Conduct comprehensive assessments of supplier capabilities, quality systems, manufacturing processes, and regulatory compliance.
• Partner with Procurement, Engineering, Manufacturing, Operations, and Regulatory teams to establish and maintain an approved supplier network.
• Drive supplier corrective actions and improvement plans to address nonconformities and ensure adherence to quality requirements.
• Serve as the primary quality representative during supplier selection, onboarding, and qualification activities.
• Provide guidance and mentorship to less experienced quality personnel on supplier quality processes and best practices.

Supplier Performance Monitoring

• Develop, maintain, and analyze supplier performance metrics, scorecards, and key performance indicators (KPIs).
• Lead supplier business reviews and supplier performance improvement initiatives.
• Conduct supplier audits to evaluate compliance with quality management systems, industry standards, customer requirements, and contractual obligations.
• Analyze supplier quality data and trends to proactively identify risks and opportunities for improvement.
• Escalate significant supplier quality concerns and risks to management while driving timely resolution.

Supplier Development and Collaboration

• Lead supplier development initiatives focused on improving quality, delivery performance, process capability, and overall supplier effectiveness.
• Provide technical guidance and support to suppliers to strengthen quality systems, manufacturing processes, and operational controls.
• Facilitate root cause investigations and corrective action activities with suppliers using structured problem-solving methodologies.
• Foster collaborative relationships with suppliers through effective communication, partnership, and joint continuous improvement efforts.
• Drive sustainable quality improvements through supplier engagement, monitoring, and performance management.

Regulatory Compliance and Documentation

• Ensure suppliers comply with applicable regulatory, customer, and industry requirements, including ISO 13485, FDA Quality System Regulation (QSR), AS9100, ISO 9001, and other applicable standards.
• Review and approve supplier-related documentation including quality agreements, qualification records, audit reports, supplier change notifications, deviation requests, and corrective action plans.
• Partner with cross-functional teams to ensure supplier-related activities are appropriately documented and maintained within the Quality Management System.
• Monitor changes to relevant regulations and standards and provide guidance regarding supplier compliance obligations.

Risk Management

• Lead supplier risk assessments and business continuity evaluations.
• Identify and assess risks associated with suppliers, materials, components, and special processes.
• Develop and implement supplier quality risk mitigation strategies and contingency plans.
• Make recommendations regarding supplier approval, probation, escalation, or disqualification based on performance and risk.
• Participate in cross-functional investigations and risk management activities to resolve supplier-related quality issues and prevent recurrence.

• Bachelor's Degree in Engineering required.
• Minimum of 4 years of experience in Supplier Quality Engineering, Supplier Development, Manufacturing Quality, or a related quality engineering discipline.
• Experience within regulated industries such as medical device, aerospace, defense, or advanced manufacturing preferred.
• Demonstrated experience conducting supplier audits and managing Supplier Corrective Action Requests (SCARs).
• Demonstrated experience leading supplier qualification, supplier monitoring, supplier development, and supplier performance improvement activities.
• Strong knowledge of quality management systems and applicable regulations, including ISO 13485, FDA Quality System Regulation (QSR), AS9100, and ISO 9001.
• Experience applying risk-based approaches and quality tools such as FMEA, 5-Why, Fishbone, 8D, Control Plans, SPC, and CAPA methodologies.
• Working knowledge of manufacturing processes such as additive manufacturing, machining, special processes, coatings, heat treatment, inspection, and related production operations preferred.
• Proven ability to investigate complex supplier quality issues, perform root cause analysis, and implement effective corrective actions.
• Excellent analytical, problem-solving, organizational, and decision-making skills.
• Strong written, verbal, and interpersonal communication skills with the ability to effectively collaborate across global cross-functional teams.
• Demonstrated ability to manage multiple priorities and projects with minimal supervision in a fast-paced environment.
• Ability to influence suppliers and internal stakeholders to achieve quality and business objectives.
• This position serves the Quality Engineering Group, which includes the need to work on export-controlled products from aerospace and defense customers.
• Ability to travel domestically and internationally approximately 25% of the time.
• Ability to work onsite in Littleton, Colorado five days per week.

Preferred Qualifications

• ASQ Certified Quality Engineer (CQE), Certified Supplier Quality Professional (CSQP), Lead Auditor certification, or equivalent professional certification.
• Experience supporting both medical device and aerospace quality management systems.
• Experience working with global suppliers and international supply chains.
• Experience with additive manufacturing technologies and related manufacturing processes.

Applications accepted online through October 29th, 2026

#LI-MP1