DescriptionWhat We Are Looking For3D Systems is seeking a highly skilled and experienced Intermediate Supplier Quality Engineer to support our global operations in Littleton, Colorado and Leuven, Belgium, serving the medical device and aerospace industries. In this role, you will be instrumental in ensuring the quality, reliability, and compliance of supplier-provided materials and components by partnering closely with suppliers and cross-functional teams worldwide. 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.
OnsiteThis role has an onsite work schedule requiring the person to be in the onsite location 5 days a week.
What You Will DoSupplier Evaluation and Qualification:- Conduct comprehensive assessments of potential suppliers to evaluate their capability to meet quality standards and regulatory requirements.
- Collaborate with the procurement team to establish and maintain an approved supplier list based on rigorous qualification criteria.
- Drive supplier corrective actions and improvement plans as necessary to address non-conformities and ensure adherence to quality standards.
Supplier Performance Monitoring:- Establish and maintain performance metrics and key performance indicators (KPIs) to monitor supplier performance and identify areas for improvement.
- Conduct regular supplier audits to evaluate compliance with quality management systems, applicable standards, and contractual obligations.
- Analyze supplier quality data and trends to proactively identify and address potential risks or quality issues.
Supplier Development and Collaboration:- Provide technical guidance and support to suppliers to enhance their quality systems, processes, and manufacturing capabilities.
- Foster strong relationships with suppliers through effective communication, collaboration, and joint problem-solving to ensure mutual success.
Regulatory Compliance and Documentation:- Ensure suppliers meet all relevant regulatory and industry standards, such as ISO 13485, FDA QSR, AS9100, or other applicable requirements.
- Collaborate with cross-functional teams to review and approve supplier-related documentation, including quality agreements, supplier audits, and corrective action plans.
- Stay updated on industry regulations and changes, providing guidance and support to ensure compliance across the supply chain.
Risk Management:- Identify potential risks within the supply chain and develop risk mitigation strategies.
- Conduct risk assessments for critical suppliers, materials, and components to ensure continuity of supply and product quality.
- Participate in cross-functional teams to resolve quality issues and implement preventive measures.
QualificationsWhat You Will Bring- Bachelor's degree in engineering, quality management, or a related field.
- Minimum of 3 years of experience in supplier quality engineering, preferably in the medical device or aerospace industry.
- In-depth knowledge of quality management systems, regulations, and standards applicable to medical devices (e.g., ISO 13485, FDA QSR) or aerospace (e.g., AS9100).
- Experience conducting supplier audits and managing supplier corrective actions.
- Familiarity with risk management principles and tools (e.g., FMEA).
- Excellent analytical and problem-solving skills.
- Effective communication and interpersonal skills to collaborate with internal and external stakeholders.
- Ability to work in a fast-paced environment and manage multiple priorities effectively.
- Willingness to travel to supplier sites as required (approximately 25% travel).
Applications accepted online through September 30th, 2026#LI-MP1
