Quality System Engineer
Company | Jabil |
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Location | Florence, KY, USA |
Salary | $Not Provided – $Not Provided |
Type | Full-Time |
Degrees | Bachelor’s |
Experience Level | Mid Level, Senior |
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.
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.
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.