Quality Engineer II

At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 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.   How will you make an impact? The Quality Engineer II is responsible for ensuring that products or services meet the required quality standards and specifications. Works with the organization’s manufacturing and engineering processes & employees, as well as with suppliers, to ensure final products are safe, reliable, and meet customer requirements while keeping the manufacturing process as effective as possible. What will you do?  General: Full use and application of principles, theories, and concepts in major field of specialization. Provides solutions to a variety of problems using standard techniques. Works under general supervision and follows established procedures. Leads small project or sub-project as part of a greater project. Primarily intra-organizational with less frequent interorganizational and outside customer contacts on routine matters. Peer recognized within work group. Specific: Responsible for applicable area’s day-to-day resolution of product dispositioning (scrap, rework, non-conformance records) through direct involvement as well as coordination with peers and other required departments or suppliers. Participate in applicable area’s Quality Improvement Committee (QIC), or equivalent operations reporting, through generation of content and/or presentation during weekly area meetings. Participate in & support favorable Quality site metrics such as CAPAs, NCs, Audits, & Complaint handling Participate in maintaining process improvement and optimization concentrating on proactive methodologies supporting defect reduction. Interface and provide technical support on quality issues with the customer as needed. Maintain appropriate documentation as required for Quality System activities. Provide technical support for successful new product transfer for established or new customers. Extended duties (if applicable) Support activities and provide mentorship to Quality Engineer I and Quality Technicians How will you get here?

Minimum Requirements: Bachelor’s or foreign equivalent degree in mechanical engineering, industrial engineering or a related field with 1-2 years relevant experience, or Bachelor’s plus Master’s degree, or 4-8 years relevant experience. Proficiency in use of personal computers, Microsoft Office products (Excel, Word, and PowerPoint) and e-mail skills required.

Requirements: Working knowledge of a manufacturing process such as Turning, Finishing, or Sterile/non-sterile Packaging. Medical device manufacturing within FDA Title 21 CFR Part 820 & ISO 13485. Gage metrology and generation of inspection plans. Identifying and leading process improvement projects. Nonconformance, CAPA, Audit observations and complaint handling. Validation experience (IQ/OQ/PQ) for product, process, equipment and/or software. Six Sigma and Lean tools such as DMAIC, SPC, process & value stream mapping. Statistical analysis that includes ANOVA, DOE, Weibull, GR&R, Capability, FMEA, KT and SPC as required. Customer requirements, specifications & change review process and incorporation. Quality documentation Change Management initiation and resolution. Proficiency preferred in use of EtQ reliance software, BabtecQ Inspection software, Windchill Change Management software, ComplianceWire Training software, Minitab or equivalent statistical software. *ISO 8 and/or ISO 9 environmental clean room interaction may be present. BENEFITS