CoorsTek Medical
  • 11-Dec-2018 to 09-Feb-2019 (MST)
  • Utah Development
  • Providence, UT, USA
  • Full Time

Medical, dental, vision, company paid & supplemental life, 401(k) with company match, and much more.


SUMMARY

Plans and oversees activities for product assurance program to prevent or eliminate defects in new or existing products by performing the following duties personally or with collaboration with other employees.  Ensures the promotion of awareness of regulatory and customer requirements throughout the organization.  This is the highest level Quality Engineer position available.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

  • Develops and implements aspects for the company quality system.
  • Responsible to improve and control regulatory/ISO compliance.
  • Analyzes, evaluates, and presents information concerning factors, such as business situations, production capabilities, manufacturing problems, economic trends, and design and development of new and existing products.
  • Develops document control and/or uses other Quality Engineers to achieve.
  • Implement alternative methods and procedures in solving problems and meeting changing market opportunities.
  • Establishes QA processes and is responsible for inspection of manufactured parts.
  • Develops initial and subsequent modifications of product designs to delineate areas of responsibility, personnel requirements, and operational procedures within program, according to and consistent with company goals and policies.
  • Devises and approves sampling procedures and controls for continuous improvement of business processes.
  • Evaluates contents of product assurance programs and confers with personnel preparatory to formulating product assurance program.
  • Visits and confers with representatives of material and component vendors to obtain information related to supply quality, capacity of vendor to meet orders, and vendor quality standards.
  • Confers with engineers about quality assurance of new products designed and manufactured products on market to rectify problems.
  • Compiles and writes training material and conducts training sessions on quality control activities.
  • Develops and implements methods and procedures for disposition of discrepant material, and devises methods to assess cost and responsibility.
  • Works overtime as needed.
  • Other responsibilities, as assigned

QUALIFICATIONS 

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

EDUCATION and/or EXPERIENCE 

High School diploma or G.E.D. and Bachelor's Degree in related field required. Prefer more than five years' related experience and/or training; or equivalent combination of education and experience.

CoorsTek Medical
  • Apply Now

  • * Fields Are Required

    What is your full name?

    How can we contact you?

    I agree to ApplicantPro's Applicant Information Use Policy.*
  • Sign Up For Job Alerts!

  • Share This Page
  • Facebook Twitter LinkedIn Email
.
Logo Values Product Development Materials Resources About Us Medical Innovation Contact Us