Supplier Quality Engineer
On-site · Indianapolis, Indiana, United States
Job Summary
Lead and author Supplier Corrective Action Requests (SCARs), ensure timely resolution and effectiveness checks; update and standardize Supplier Quality procedures to align with company and regulatory expectations; manage and track supplier quality metrics and KPIs, identifying trends and areas for improvement; support development of dashboards and reporting tools to improve visibility into supplier performance; conduct and support supplier audits (on-site and/or remote) to ensure compliance with quality standards; collaborate cross-functionally with Quality, Regulatory, and Operations teams during commercialization activities; ensure supplier-related processes are compliant with QMS requirements and industry regulations; drive continuous improvement initiatives within supplier quality processes.
Required Qualifications
- 5+ years of experience in Supplier Quality within the pharmaceutical or life sciences industry
- Hands-on experience writing and managing SCARs / CAPAs
- Experience conducting supplier audits
- Strong working knowledge of Quality Management Systems (QMS)
- Experience supporting commercialization or product launch activities
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