Analyst I, Quality
BaxterRound lakeUpdate time: October 2,2019
Job Description

Around the world, our employees are united by our mission to save and sustain lives. Together, we create a culture that encourages colleagues to pursue rewarding careers -- where everyone has the opportunity to do meaningful work as a part of a team they respect, in an environment that values each person’s contributions. We’re happy you’re interested in continuing your career journey with Baxter.

Summary

The Quality Analyst I plays a key role in supporting the supplier requirements review process for the Baxter Supplier Quality team. The Quality Analyst I leads periodic supplier requirement reviews, identifies and resolves gaps, and maintains supplier qualification files in Baxter’s electronic supplier quality database. The Quality Analyst I acts as a liaison for the Supplier Quality team to global facilities, businesses, and regions.

Essential Duties and Responsibilities

  •     Lead periodic supplier requirement reviews by confirming and/or obtaining quality requirements such as quality agreements, surveys, or quality certificates. Obtain resolutions for areas identified as compliance issues.
  •     Own and manage new supplier requests for low risk suppliers.
  •     Interpret and execute policies and procedures that affect the organizational unit.
  •     Utilize electronic systems for maintaining supplier quality records and uploading requirements.
  •     Carry out activities for acquisitions, divestitures, and remediation under established operating procedures and protocols.
  •     Interact frequently with functional peer groups, area management, and Baxter’s suppliers.

Qualifications

  • Strong interpersonal skills and attention to detail
  • Team player with proven problem solving skills, and strong verbal and written communication skills
  • Must be able to handle multiple projects concurrently and prioritize workload
  • Computer experience with Microsoft Office/Sharepoint applications and web-based database systems
  • Working knowledge of medical device and pharmaceutical standards and regulations (FDA, ISO, ICH) strongly preferred

Education and/or Experience

  • Bachelor’s degree in science, engineering or another technical area. Alternately, a combination of equivalent education and experience will also be considered.
  • 1 – 3 years of experience working in the pharmaceutical or medical device industry.
  • Prior experience working with TrackWise is preferred.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
                                                                                                                                                               
EEO is the Law 
EEO is the law - Poster Supplement

Pay Transparency Policy

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to Americas_TTA@baxter.com and let us know the nature of your request along with your contact information.

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