Supplier Quality Specialist

Posted Yesterday
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Hiring Remotely in Illinois, USA
Remote
79K-119K Annually
Junior
Other
No.1 privately held manufacturer & distributor of health care products in the U.S.
The Role
Manage vendor onboarding and re-evaluation, maintain supplier audit schedules, coordinate third-party laboratory testing, analyze supplier quality data, prepare assessment reports, monitor supplier performance, and support process improvements within medical device/pharmaceutical supplier quality programs.
Summary Generated by Built In

Job Summary

Manage the vender set-up process, including initial vendor approval and routine re-evaluation. Serve as a subject matter expert in Medline’s vendor evaluation process. Will also be responsible for coordination of third-party laboratory testing.

Job Description

Responsibilities

  • Review, approve, and upload documentation for initial approval of new Medline vendors. Review, approve, and upload documentation for re-evaluation of Medline vendors.

  • Act as a Subject Matter Expert (SME) on Medline’s vendor evaluation program.

  • Maintain Medline’s supplier audit schedule, by adding audit requests to the audit schedule and working with the audit team to ensure audits are completed according to schedule.

  • Analyze and compile reports on a routine basis related to Supplier Quality.

  • Prepare reports on assessment activities, findings, and outcomes. Coordinate third party testing between product divisions and third-party testing laboratories, including negotiating pricing, service level agreements and determining the appropriate product testing to be performed.

  • Monitors supplier performance and supports efforts to develop and implement changes for process improvement.

Requirements

  • Education Typically requires a Bachelor's degree in Chemistry, Biology, or related science field.

Work Experience

  • At least 2 years of experience in a medical device or pharmaceutical related field.

Knowledge/Skills/Abilities

  • Time management skills to prioritize, organize, and track details in order to meet deadlines of multiple projects.

  • Experience using MS Office Suite products (Word, Excel, PowerPoint, Outlook). Position requires up to 25% travel

Preferred skills

  • Knowledge of FDA requirements and experience with FDA. Knowledge of ISO 13485 requirements. Experience with supplier approvals, evaluations, re-evaluations, and monitoring

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.

The anticipated salary range for this position:

$79,000.00 - $119,000.00 Annual

The actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.

We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

Skills Required

  • Bachelor's degree in Chemistry, Biology, or related science field
  • At least 2 years of experience in a medical device or pharmaceutical related field
  • Experience using MS Office Suite (Word, Excel, PowerPoint, Outlook)
  • Time management skills to prioritize, organize, and track details across multiple projects
  • Ability to travel up to 25%
  • Knowledge of FDA requirements and experience with FDA
  • Knowledge of ISO 13485 requirements
  • Experience with supplier approvals, evaluations, re-evaluations, and monitoring
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The Company
HQ: Northfield, IL
20,000 Employees
Year Founded: 1961

What We Do

All across America and the world, we help healthcare systems improve patient outcomes and reduce costs through clinical and financial solutions. As both a manufacturer and distributor of medical devices and supplies, we’re made up of problem solvers. Risk-takers. Big thinkers and doers.

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