Sr. Quality Systems Engineer

Job Description
This professional is responsible for Product Team Support for Quality System Design and Audit for support of steady state manufacturing processes, including conducting audits to FDA, GMP, ISO13485 and any other applicable standards and providing compliance assessment and status. The position is located in our Southington, CT manufacturing facility where we are a worldwide leader in offering an extensive variety of safety and conventional I.V. catheters.
REQUIREMENTS
Must have a minimum of 5 years quality engineering experience with CQE, CRE, CQA, and/or PE training/certification; a Bachelor's degree in Engineering (Mechanical/Electrical/Industrial) is preferred. Six Sigma high desired. A minimum of two years related work experience in a medical device area is highly preferred along with compliance to FDA, GMP, ISO 13485 any other applicable standards. We will consider candidates with a related Master's degree and 3 years experience.

Company Info
For more than 2 decades, Smiths Medical has produced medical devices that positively impact the lives of people worldwide. Our commitment to lead the industry in the development of medical devices to improve patient's lives is evident in the quality products we have introduced to the market. A member of Smiths Group plc, one of the UK's largest corporations, Smiths Medical is well positioned to invest in continuous improvement, technological innovation and customer service.

In addition to a career with a company dedicated to your success & professional development, we offer a competitive salary & generous benefits.

To apply online, visit our website at
www.smiths-medical.com/careers www.smiths-medical.com/careers

Smiths Medical is an Equal Opportunity Employer.
Drug Free Workplace/MFDV