Senior Supplier Quality Engineer — Global Quality Leader (Onsite)

Morgan Stanley; Littleton (CO); Sur place; USD 85 000 - 100 000; Plein temps

Résumé du poste

3D Systems in Littleton, Colorado is seeking a Senior Supplier Quality Engineer to lead supplier quality strategy, development, and risk management across the supply chain, supporting medical device and aerospace industries.

You will manage supplier audits, performance metrics, and cross-functional collaboration with Procurement, Engineering, Manufacturing and Regulatory to ensure regulatory compliance (ISO 13485, FDA QSR, AS9100, ISO 9001). Travel ~25% and onsite five days a week.

Qualifications

• 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 with ISO 13485, FDA QSR, AS9100, ISO 9001 and related regulations.

Responsabilités

• Lead supplier evaluation, qualification and onboarding activities.
• Drive supplier development, CAPA, and corrective actions with cross-functional teams.
• Perform supplier audits and manage supplier performance metrics and risk assessments.
• Collaborate with Procurement, Engineering, Manufacturing, and Regulatory teams to ensure compliance.
• Lead risk-based supplier quality initiatives and continuous improvement programs.
• Travel approximately 25% domestically and internationally.
• Work onsite in Littleton, Colorado five days per week.

Connaissances

Supplier quality

Auditing

Root cause analysis

Problem solving

Regulatory knowledge

Cross-functional collaboration

Travel readiness

Formation

Bachelor's Degree in Engineering

Description du poste

3D Systems in Littleton, Colorado is seeking a Senior Supplier Quality Engineer to lead supplier quality strategy, development, and risk management across the supply chain, supporting medical device and aerospace industries.

You will manage supplier audits, performance metrics, and cross-functional collaboration with Procurement, Engineering, Manufacturing and Regulatory to ensure regulatory compliance (ISO 13485, FDA QSR, AS9100, ISO 9001). Travel ~25% and onsite five days a week.