Quality Systems Engineer

2 settimane fa

Florence, Toscana, Italia Jabil Circuit A tempo pieno

Now offering a $2,000 Sign-On Bonus to new hires for this position on our Jabil Team

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

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 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.

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 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.

How will you get here?

Education and Experience:

  • 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.

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.

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