At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the worlds 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.

Now offering a $2000 SignOn Bonus to new hires for this position on our Jabil Team!

Jabils 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!

Job Summary:
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 companys quality management systems (QMS) in alignment with ISO9001 industry standards and customer requirements. This individual will work closely with crossfunctional teams to ensure compliance with regulatory requirements and the continuous improvement of product quality across various stages of production.

How will you make an impact

This role is crucial in ensuring that the organization maintains a high standard of quality in its products and services while adhering to regulatory requirements and industry best practices.

What will you do

• Develop implement and maintain the companys 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 nonconformities 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 crossfunctional teams to investigate and resolve customer complaints or quality issues.

• Conduct training on qualityrelated topics and QMS procedures for employees.

• Monitor and manage product inspection testing and validation activities.

How will you get here

Education and Experience:

• Bachelors 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 35 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 problemsolving and communication skills.

• Ability to work crossfunctionally and manage multiple projects simultaneously.

Knowledge Skills Abilities:

• Strong attention to detail and organizational skills.

• Excellent written and verbal communication skills.

• Ability to interpret and apply quality standards and regulations.

• Proficiency in using Microsoft Office tools.

• Ability to work independently and as part of a team.

• Knowledge of continuous improvement methodologies (e.g. Lean Six Sigma).

Preferred Qualifications:

• 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.

BE AWARE OF FRAUD: When applying for a job at Jabil you will be contacted via correspondence through our official job portal with a jabil email address; direct phone call from a member of the Jabil team; or direct email with a jabil email address. Jabil does not request payments for interviews or at any other point during the hiring process. Jabil will not ask for your personal identifying information such as a social security number birth certificate financial institution drivers license number or passport information over the phone or via email. If you believe you are a victim of identity theft contact the Federal Bureau of Investigations internet crime hotline (3 the Federal Trade Commission identity theft hotline () and/or your local police department. Any scam job listings should be reported to whatever website it was posted in.

Jabil including its subsidiaries is an equal opportunity employer and considers qualified applicants for employment without regard to race color religion national origin sex sexual orientation gender identity age disability genetic information veteran status or any other characteristic protected by law.

Accessibility Accommodation

If you are a qualified individual with a disability you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil/Careers site as a result of your disability. You can request a reasonable accommodation by sending an email to or callingwith the nature of your request and contact information. Please do not direct any other general employment related questions to this email or phone number. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.

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