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Baxter International

Global provider of medical care products

Global Regulatory Affairs Publishing Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRound Lake, IL, USA$72k - $99k /yr

About the Job

Requirements

  • A bachelor's degree or an equivalent combination of education and relevant professional experience is required.
  • Hands-on experience with pharmaceutical submissions and electronic Common Technical Document (eCTD) submissions, including Investigational New Drug applications (INDs), Biologics License Applications (BLAs), New Drug Applications (NDAs), Abbreviated New Drug Applications (ANDAs), and device submissions (eCopy and eStar).
  • Experience with electronic publishing, document, or data management systems such as Veeva/RIM, ISI Toolbox, or eCTD Xpress.
  • Familiarity with electronic submission regulations and guidance, including 21 CFR Part 11.
  • A sound basis of regulatory knowledge is required.
  • Ability to manage complex projects and timelines in a matrix team environment.
  • Strong oral and written communication and presentation skills.
  • Demonstrated interpersonal and negotiation skills.
  • Ability to independently identify compliance risks and escalate them when necessary.

Responsibilities

  • Manage the preparation of regulatory submissions for major markets, including the United States, European Union, Canada, Australia, and other global regions.
  • Perform technical validation and resolve publishing errors before dispatch.
  • Support initial applications and lifecycle submissions.
  • Drive the integration and transition of products into regulatory operations processes.
  • Compile technically compliant submission components and manage document formatting.
  • Represent Global Publishing on project teams when needed, driving timelines for submission document deliverables.
  • Partner with functional peer groups inside and outside the department.
  • Provide system and process support, development, and training when necessary.

Desired Qualifications

  • 1–3+ years of regulatory publishing or regulatory operations experience in the pharmaceutical or medical device industry would be an advantage.

About the Company

Baxter International

Global provider of medical care products

Baxter International develops and manufactures medical products and equipment for hospitals and blood banks. Its products include sterile IV solutions and blood storage containers; innovations like the Transfuso-Vac extended blood shelf life, and a plastic blood bag helped shape modern blood banking. The company differs from competitors through a long track record of sterile manufacturing, blood-storage innovations, and strategic mergers that broaden its product portfolio. Its goal is to provide reliable, safe medical products that support patient care and hospital operations worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Deerfield, IL
Founded
1931

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