Quality Engineer III

The Quality Engineer III leads the development and implementation of quality plans, programs, and procedures using quality control statistics, lean manufacturing concepts, and analyses. Ensures that performance and product quality conforms to established company, customer and regulatory requirements. Reviews, analyzes, and reports on quality discrepancies related to assembly and process. Investigates problems and recommends disposition, modification, and corrective action for recurring or non-recurring discrepancies. Interfaces with site management, manufacturing, engineering, customer, vendor, and subcontractor representatives to ensure requirements are met.

• Develops, modifies, applies, and maintains quality evaluation and control plans and protocols for processing materials into partially finished or finished products.
• Analyzes inspection and testing processes, mechanisms, and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for, products or materials that do not meet required standards and specifications.
• Audits quality systems for deficiency identification and correction.
• Confirms that corrective measures meet acceptable reliability standards, and that documentation is complete and compliant with requirements.
• Develops methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.
• Writes, reviews, approves process validations/qualifications, facilitates resolution of validation deviations in accordance with Jabil and customer requirements.
• Evaluates, makes recommendations, and implements changes to the validation and qualification program as part of continual improvement or remediation activities.
• Supports and champions change controls in relation to customer, supplier, and internally driven changes.
• Leads team to ensuring that corrective actions (CAPA) are completed in accordance with relevant ISO/regulatory body requirements, Jabil procedures, and that documentation is complete and compliant with requirements.
• Leads investigation team, and documents response in ensuring timely resolution of customer complaints.
• Leads continuous improvement efforts; Has a quality-first mentality; Applies internal and external best practices to apply to her/his work.
• Support all company safety and quality programs and initiatives.
• Mentoring of Quality Engineers and training employees in the requirements of Quality.
• Role model and promote the organizations Values and Behaviors.
• When documented appropriately, can hold delegation authority for Quality Engineering Supervisor.
• Other responsibilities may be assigned from time to time as needed, based on the evolution of the company and the requirements of the department/position.

• Degree in Science/ Engineering or equivalent experience (High School degree or GED certificate & 7+ years of direct experience in lieu of Degree).
• 5+ years of relevant medical device or injection molding experience.
• Must be knowledgeable in the operation of 13485 and/or ISO 9001 Quality Management Systems.
• Experience in automated assembly solution, cleanroom manufacturing experience preferable.
• ASQ CQE, desirable. Lean Six Sigma experience.
• Strong Computer Skills. Proficiency in use of personal computers, Microsoft Office products (Excel, Word, and PowerPoint) and email skills required.
• Frequent sitting, standing and walking with occasional lifting of up to 25 lbs.

*This position is not eligible for immigration and/or visa sponsorship. Applicants must be legally authorized to work in the United States without current or future sponsorship by Jabil. Applicants requiring sponsorship will not be considered.