Quality Engineer - (NCR / CAPA and SAP REQUIRED)
- Location : ONSITE - Ladson, SC (29456)
- Duration : 9 – 11 months – estimated to end 12 / 31 / 2025 – (Contract extension potential)
- Type : W2 contract (Third-party or C2C "Corp-to-Corp" arrangements WILL NOT be considered for this role)
- Pay : Negotiable depending on direct-related experience
- Work Authorization : Must be currently in the United States with active employment authorization documents. Visa sponsorship is not available, now or in the near future, for this position.
- Hours : Monday to Friday 8 : 00AM to 5 : 00PM
Summary
In this contract role, is under our Commitment to Quality Program. The Quality Engineer– CtQ role is responsible for the implementation of materials master, receiving inspection plans and regulatory compliance to ensure our products meet the highest standards of quality and safety. This role works closely with cross-functional teams to create, maintain and improve our quality management systems, ensuring compliance with ISO 13485, and other regulatory requirements.
Key Responsibilities Commitment to Quality
Develop, implement, and maintain robust quality systems and procedures in line with ISO 13485, MDSAP Certifications and other industry standards.Perform assessments to ensure adherence and commitment to quality specifications and regulatory requirements.SAP Quality Management (QM) Integration
Create inspection plans in SAPUse the SAP QM module to manage inspections plans, record quality data, and document quality notifications.Ensure accurate data capture and traceability of quality-related information throughout the product lifecycle.Set up materials-master maintenance and complete system data correction in SAP fields and inventory locations to ensure data accuracy and warehouse optimization.Collaborate with IT, Planning, Supply Chain and production teams to optimize SAP processes for quality management.Inspection and Testing
Provide oversight for inspections and tests of raw material, components, and assist with finished product inspections using industry standard techniques.Review and interpret technical documents, including design specifications, engineering drawings, and regulatory standardsRisk Management & Continuous Improvement
Assist with product quality investigations, root cause analysis and CAPA facilitation to address quality issues.Supports risk management activities, including risk assessments and mitigation plans in compliance with design controls.Supports process improvements and facilitates PDCA process for productionAssists with Non-Conforming Material process.Qualifications & Skills
Demonstrates high level analytical skills to identify improvement opportunities and develop workable solutions to resolve complex problemsStrong attention to detail and the ability to work collaboratively in a cross-functional team.Proactive mindset with a commitment to continuous improvement.Experience :
3 years of experience in a quality engineering role or an equivalent level of knowledge in medical devices.Proven hands-on experience with SAP, particularly the quality management module.Important information : To be immediately considered, please send an updated version of your resume to Deas172@kellyservices.com.
Kelly does not expense relocation / interview costs)Work Authorization : Must be able to work in the United States with current employment authorization documents without VISA status that require Visa sponsorship now or in the future.
In addition to working with the world’s most recognized and trusted name in staffing, Kelly employees can expect :
Competitive payPaid holidaysYear-end bonus programRecognition and incentive programsAccess to continuing education via the Kelly Learning Center
