Quality Manufacturing Engineer

Philips•Murrysville, PA

1d•$92,000 - $128,000•Onsite

About The Position

In this role you are responsible for providing facilitation in achieving a state of high-quality performance and compliance in the factories and aid in providing oversight of Philips processes utilized in manufacturing.

Requirements

Bachelor's / Master's Degree in Mechanical Engineering, Electronics Engineering, Science or equivalent.
3+ years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering or equivalent.

Nice To Haves

Experience with medical device regulations and standards
Process Quality Management
CAPA
Root Cause Analysis
Data Analysis

Responsibilities

Facilitates operations performance monitoring, reporting, improvement and development, facilitates improvement programs in factory, and supports analytical testing and Supplier Quality Engineering (SQE), Supplier Quality Assurance (SQA) and Purchasing.
Conducts assessment of impact to Process Failure Mode and Effects Analysis (PFMEA) and associated controls in relation to design changes and assists in Manufacturing Process Development and Design Transfer activities.
Leads analysis of defects for determining dispositions of non-conformances, drives management of Non-Conformances (NC) and Quality Notifications (QN) and facilitates implementation of effective Corrective and Preventive Actions (CAPA) actions.
Facilitates timely quality engineering and quality assurance tasks, ensures manufacturing quality systems are maintained, handles single or complex process validation and process improvement activities, and helps in completion of New Product Introduction (NPI) and product transfers in factory.
Leads validation protocols, facilitates production builds to support validation activities, analyzes data for reports, process improvement initiatives, and validation activities.