QMS Engineer

Jabil • Florence, KY

75d

About The Position

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe. Jabil's Florence, KY facilities located in the Cincinnati Northern KY area are experiencing growth to support the manufacturing of servers. We are actively hiring to increase production and to support our 7/24 operation. Please apply if you want to join a growing team! In this position reporting to the Site Quality Management Systems Manager the Quality Systems Engineer will be responsible for supporting the development, maintenance, and improvement of the company's quality management systems (QMS) in alignment with ISO9001 industry standards and customer requirements. This individual will work closely with cross-functional teams to ensure compliance with regulatory requirements and the continuous improvement of product quality across various stages of production.

Requirements

• Bachelor's degree preferred in Engineering, Quality Management, or a related field.
• Professional certifications (e.g., Six Sigma, ASQ, or ISO 9001 Lead Auditor) preferred.
• At least 3-5 years of experience in quality engineering, quality systems, or a related field, preferably within manufacturing or production environments.
• Strong knowledge of quality management systems, methodologies, and tools (e.g., root cause analysis, corrective/preventive actions, FMEA, SPC).
• Experience with ISO 9001 and other relevant standards.
• Excellent analytical, problem-solving, and communication skills.
• Ability to work cross-functionally and manage multiple projects simultaneously.

Nice To Haves

• Experience in a specific industry such as automotive, medical devices, or pharmaceuticals.
• Familiarity with quality control tools and techniques, such as statistical analysis, process control, and failure mode effects analysis (FMEA).
• Experience in leading audits and managing CAPA (Corrective and Preventive Action) processes.

Responsibilities

• Develop, implement, and maintain the company's Quality Management System (QMS), including procedures, policies, and documentation.
• Ensure compliance with ISO 9001, ISO 13485, FDA regulations (if applicable), and other relevant quality standards.
• Perform audits and inspections to ensure adherence to internal processes and external regulatory standards.
• Facilitate root cause analysis and corrective actions for non-conformities or quality issues.
• Coordinate and support the preparation of documentation for product certifications, audits, and regulatory submissions.
• Analyze and report quality performance metrics and trends, providing recommendations for improvement.
• Collaborate with engineering, manufacturing, and supply chain teams to drive quality improvement initiatives.
• Support the design and development of new products by ensuring that quality standards are integrated from the beginning.
• Lead or participate in cross-functional teams to investigate and resolve customer complaints or quality issues.
• Conduct training on quality-related topics and QMS procedures for employees.
• Monitor and manage product inspection, testing, and validation activities.

What This Job Offers

• Industry: Computer and Electronic Product Manufacturing
• Education Level: Bachelor's degree
• Number of Employees: 5,001-10,000 employees