Job Description Help for Job Description. Opens a new window. Must have the following in order to apply: College degree Three (3) years of experience Manufacturing quality engineering experience Experience conducting audits and inspections Valid driver's license

Preferred Qualifications:

Bachelor's degree in engineering or related field preferred

Skills:

Knowledge of ISO 13485 and FDA regulations (QMSR)

Required Screenings:

Drug Testing/Screening (Pre-Employment); Background Checks (

Local, State & Federal:

5-Year History Check); Reference Checks. Maintain and improve Quality Management System (ISO 13485, FDA QMSR) and support regulatory compliance Perform quality audits, First Article Inspections (FAIs), and assist with routine receiving inspections of vendor components Analyze quality data and implement corrective and preventive actions Partner with cross-functional teams to improve manufacturing processes

Work Environment:

Indoor office and production-floor environment; business-casual attire, including closed-toe shoes, jeans or trousers, and a polo or button-down shirt. Will be discussed with applicant.

Hiring Process:

Submit resume via email. In order to apply to this position, please click "Apply" located at the top of the job order page, and you will receive the employer contact information. Employer has indicated the means listed are the only means they will accept to apply.

Days & Hours:

Full Time position; Monday through Friday; 1st shift (8:00am to 4:30pm); 40 hours per week. Complete work schedule will be discussed with applicant.

Pay:

$65,000 to $80,000 per year; depends on experience. Benefits are offered. Drug Free Workplace