Responsible for the design development and implementation of standards methods and procedures for inspecting testing and evaluating the precision and accuracy of company products in compliance with contractual and regulatory requirements.
Performs analysis on reported nonconformities and discrepancies related to assembly process mechanical electrical electro-mechanical systems field and clinical data.
Further investigates the cause for discrepancies and nonconformities to develop disposition and recommend corrective action plans. Leads material review board and Process Failure Mode Effects Analysis (PFMEA) activities.
Interfaces with manufacturing engineering customer vendor and subcontractor representatives to ensure requirements are met. Conducts program quality cost account management and manages supplier corrective actions.
Serves as the primary interface to customers and supplier for quality related matters.
Senior professional with strong knowledge of job area and broad knowledge of project management.
Manages complex projects or processes with general oversight.
Communicates within and outside of own function to gain cooperation on operational processes practices and procedures.
Makes moderate to substantial improvements to systems and processes.
Contributes to achievement of departmental goals and operating plans with direct impact on the departmental results.
Requirements:
BS/4-year degree in technical field (mechanical/electrical engineering).
Working as QEs for corrective action continuous improvement.
Helping with Impending move from Phili to Camden working on open corrective actions MRB (material review board) commissioning NCs (Nonconforming).
Must- Have:
4-5 years prior QE experience (Able to hit the ground running).
Knowledge of root cause and corrective actions.
Process Failure Mode Effects Analysis (PFMEA) activities.
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