Join the world's leading eye care company with sales of $5.6 billion in 2007. The company’s nearly 13,000 employees worldwide, work in 75 facilities around the world to research, develop, manufacture and sell eye care products in more than 180 countries. The Company is the largest specialty eye care company in the world and leads the growing $14.5 billion market for eye care products. The Company has delivered strong and stable growth for over 60 years, and it is positioned to build on this record in the years to come. For ten consecutive years, Fortune magazine has selected company as "One of the 100 Best Companies to Work For". U.S. Operations is headquartered at its 300-acre campus located in Fort Worth, Texas.

The Huntington IOL Facility is located in Huntington, West Virginia, along the Ohio River, and is the world's leading intraocular lens (IOLs) manufacturing facility. Over 750 employees produce more than half of the IOLs implanted worldwide.

The company is currently looking for a Quality Engineering Section Manager for their Huntington West Virginia Facility.

BASIC JOB FUNCTION:
The person in this position will manage the Quality Engineering staff and resources in order to plan, implement, and coordinate studies for quality/process improvement, equipment upgrades and cost reduction; ensure timely and efficient handling of complaint processing; and facilitate new product and process introduction for the Huntington facility. This person will manage Calibrations/Metrology, Incoming Quality Assurance (IQA), Customer Complaint Processing, Supplier Quality and other quality engineering functions.

MINIMUM QUALIFICATIONS:
Bachelor’s degree from an accredited institution in Engineering, Mathematics, or a related discipline. Ten (10) years statistical Quality Assurance experience in the medical device or related field having comparable technology and regulatory requirements with at least two (2) years at a supervisory level. PC proficiency, report writing expertise and highly developed interpersonal skills.

PREFERRED QUALIFICATIONS:
Master’s degree from an accredited institution in Engineering, Mathematics, or a related discipline; or Bachelor’s of Science in Chemistry with applied statistics. Ten (10) years statistical Quality Assurance experience with at least two years at a supervisory level in the medical device or related field having comparable technology and regulatory requirements. PC proficiency, report writing expertise and highly developed interpersonal skills.

BENEFITS:
Companies benefits package includes a competitive salary, the 401(k) Plan which matches employee contributions up to 5% of eligible pay at the rate of $1.00 for each dollar contributed, and the company Retirement Plan (ARP), a qualified plan in which company contributes 7% of eligible pay to the accounts of all eligible employees. By combining the Company's contributions to the 401(k) and ARP, employees can receive up to 12% of eligible pay towards retirement.  Also offers medical, dental, vision, life and disability coverage, an on-site fitness center and much more. Consider having all this in a fast paced environment within a stable world-class organization.

Send a word resume to jthompson@tescareers.com
Jeff Thompson
TES, Inc
440-266-0022 ext 104