Senior Specialist, Quality Engineer

L3Harris•Camden, NJ

16d

About The Position

Manufacturing Quality Engineers are a key component to manufacturing defect free products and ensuring that our process is as efficient as possible. This is an excellent opportunity for an individual with a strong quality background, interested in driving quality into our product. The Manufacturing Quality Engineer will work primarily in support of the Operations Department production floor daily operations and will report to the Associate Manager, Quality Engineering.

Requirements

Bachelor’s Degree and minimum 6 years of prior relevant experience. Graduate Degree and a minimum of 4 years of prior related experience. In lieu of a degree, minimum of 10 years of prior related experience.
Proficiency in MS Office software (Excel/Outlook/Word/PowerPoint, etc.)
Knowledge of Geometric Dimension and Tolerancing (GD&T)
Familiarity with the MRB Process and working in a Manufacturing environment.
Knowledge of RCCA processes and methodology
Demonstrated experience working in an ISO9001 or AS9100 environment

Nice To Haves

Bachelor’s Degree in an Engineering discipline
ASQ certification (CQT, CQI, CQE, CMQ/OE) or demonstrated application of these principles on programs.
Experience working with IPC-J-STD-001 and IPC/WHMA-A-620 a plus
Experience working with the QMS functions within SAP
Experience using Coordinated Measuring Machines (CMM) a plus

Responsibilities

Effectively communicate issue descriptions, improvement progress, and latest status to management
Collaborate across multiple disciplines to find root cause for systemic failures and implement corrective actions.
Lead/support in-depth investigations of quality issues (Non-Conformances, Process Problems, RCCA’s, Audit Observations, etc.) ensuring effective corrective/preventive actions occur.
Participate in CI/LEAN initiatives and utilize Six Sigma tools for process improvements (8-D, Fish-bone diagram, KNOT chart, 5 Why’s, etc.)
Participate in cross-functional teams for process control, improvement, and optimization projects; participate in ad-hoc continuous improvement projects
Maintain strong working knowledge of current ISO 9001 requirements and support the development, implementation, and monitoring of the QMS
Address Nonconformance reports, including dispositions, RCCA, Escapes and approval of Supplier FAI
Manage/collaborate in the Material Review Board process