QA Engineer III

posted:
Location
Murrysville, Pennsylvania
Industry
Manufacturing & Production
Job Type
Temporary
Salary
US$ 45.00 - US$ 50.00 per hour
Ref. Number
RUGPHI306
Contact
Spherion Staffing , Spherion
Phone
724-334-3113
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Job Description

Independently Produces and completes Supplier Quality Engineering related activities and documentation. • Completes Qualification of materials and components (including spare parts), development/ improvement of supplier processes for CtQ's, supplier process control plans; ensuring that the supplied part meets specifications, and the control limits/tolerances for CtQ parameters are met. • Qualifies and sustains subprocesses of suppliers, including performing process validations for critical supplier processes impacting part quality. • Ensures that the components/products at the supplier (including spare parts and services) are released according agreed specification and quality requirements (APQP /PPAP), and SQ audit results. • Executes SCAR management, effective and timely closure and Review/risk assessment of QN's and their escalation to SCARs where needed. • Independently works to deploy common approaches and working methods to drive ‘’One Philips’’ towards Supply Base in the assigned BG or Market A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. • This job is a fully qualified, career-oriented, journeylevel position. • Has a complete knowledge of company products and services. • Frequently interacts with subordinate supervisors, customers, and/or functional peer group managers, normally involving matters between functional areas, other company divisions or units, or customers and the company. Often must lead a cooperative effort among members of a project team Works on issues of diverse scope where analysis of Works on issues of diverse scope where analysis of situation or data requires identification and evaluation of a variety of factors, including an understanding of current business trends. • Follows processes and operational policies in selecting methods and techniques for obtaining solutions. • Acts as advisor to subordinates to meet schedules and/or solve technical problems. • Develops and administers schedules, performance requirements. • Probably has a budget responsibility. 

Skills

Mid-level SQE Regulated industry experience - ISO 13485 / FDA Manufacturing experience Root cause analysis Corrective and Preventive action Excellent communication skills Sense of urgency Ability to build relationships

Qualification

Bachelor’s degree in an engineering or science discipline, or equivalent experience. 8-10 years of total industry experience with 4+ years of related experience in a medical device or regulated industry preferred. • • Experience in root cause analysis, corrective and preventive action methods. • Expertise/experience in problem solving with quality tools such as: 6-sigma / 8-D / CAPA / FMEA/ 5WHY etc. • Good knowledge of production/quality development and control methods; CtQ definition, DfSS, SPC, APQP, FMEA, Control Plans, etc.) 

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