Supplier Quality Engineer

Key Responsibilities Support and maintain the Supplier Quality Program in compliance with applicable regulatory requirements. Perform supplier evaluations, including risk assessments, questionnaires, and supplier audits as needed. Issue supplier quality complaints and drive corrective and preventive actions to resolution. Develop, review, and maintain Supplier Quality Agreements. Assess supplier and vendor changes, coordinate cross-functional reviews, and track implementation. Participate in internal quality audits and monitor corrective action effectiveness. Support regulatory inspections and customer audits. Maintain supplier quality documentation, including electronic filing and document management. Execute assigned quality projects within established timelines. Promote a safe, compliant, and quality-focused work environment. Qualifications Bachelor's degree in Life Sciences, Engineering, or a related technical field (or equivalent experience). 3+ years of Supplier Quality or Quality Assurance experience within pharmaceutical, biotech, medical device, or other regulated manufacturing environments. Strong understanding of cGMP regulations and quality systems. Experience with: Supplier Quality Management Quality Agreements Change Control CAPA Internal Audits Deviations Complaint Investigations Document Control Experience using statistical tools for quality analysis. Proficiency with Microsoft Office. Strong analytical, problem-solving, organizational, and communication skills. Ability to manage multiple priorities in a fast-paced manufacturing environment. Experience working cross-functionally with suppliers and internal stakeholders. #J-18808-Ljbffr