Supplier Quality Engineer

Overview We are seeking a motivated and detail-oriented Supplier Quality Engineer (Entry Level) to support quality engineering systems, methodologies, and compliance activities within a regulated manufacturing environment. This role plays a critical part in ensuring product quality, regulatory compliance, and continuous improvement while partnering cross-functionally to support operational excellence and new product development. The Quality Engineer will serve as a key quality representative, supporting internal teams, suppliers, and stakeholders to strengthen quality systems and drive measurable improvements across manufacturing and supplier operations. Responsibilities Quality Engineering & Process Control: Develop, implement, and maintain effective process control systems to support product development, qualification, and ongoing manufacturing. Lead and support implementation of assurance activities, process controls, and CAPA systems to meet internal, customer, and regulatory requirements. Apply structured problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues. Support development and execution of streamlined business systems to proactively identify and resolve quality risks. Act as a quality leader and advocate across cross-functional teams to drive quality culture and best practices. Supplier Quality Engineering Drive supplier quality performance through Part Quality Plan (PQP) implementation and ongoing supplier engagement. Review, approve, and facilitate supplier PQP submissions for purchased products. Lead supplier qualification and selection through robust audit and assessment processes. Ensure supplier compliance with Quality Management System (QMS) and regulatory requirements. Lead and monitor supplier CAPA development and execution to ensure sustained quality improvements. Quality Systems & Compliance Build quality into all aspects of work by maintaining compliance with internal quality systems and external regulatory requirements. Support regulatory assurance, audit readiness, and continuous improvement initiatives. Required Qualifications Bachelor’s Degree in Engineering or related technical discipline (OR non-technical degree with 5+ years of relevant manufacturing, engineering, or quality experience) Minimum 3 years of experience in manufacturing, engineering, quality assurance, or regulatory assurance Strong problem-solving and root cause analysis skills Preferred Qualifications ASQ Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA) Demonstrated experience with Quality Management System (QMS) tools and continuous improvement methodologies Prior supplier quality experience within the medical device or regulated manufacturing industry #J-18808-Ljbffr Select Source International