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Grifols

Plasma Regulatory Affairs Associate

Grifols

Plasma Regulatory Affairs Associate overseeing licensing and regulatory compliance in the plasma industry. Preparing applications, maintaining compliance, and collaborating with regulatory authorities for a global healthcare company.

Posted 5/16/2026full-timeResearch Triangle Park • North Carolina • 🇺🇸 United StatesJuniorMid-LevelWebsite

About the role

Key responsibilities & impact
  • Accurately prepare regulatory applications required by federal and other regulatory authorities.
  • Research internal documents, complete applications, and forms; prepare cover letters and summaries.
  • Submit and monitor application submission for timely review and acceptance.
  • Provide updates to management on the status of applications.
  • Maintain applicable shared mailboxes, dashboards and accounts related to administrative licensing activities.

Requirements

What you’ll need
  • Bachelor's Degree in a scientific discipline (e.g., Pharmacy, Chemistry, Biology).
  • Preferred two (2) years related technical and/or regulatory experience in pharmaceutical or blood industry.
  • Experience with Microsoft Office.
  • Experience with Adobe PDF.
  • Experience in plasma collection, pharmaceutical industry, or a regulated field.

Benefits

Comp & perks
  • Professional behavior with internal/external business associates, reflecting positively on the company.
  • Quality awareness of potential compliance defects in their area of responsibility.
  • Skills in managing multiple tasks with competing demands and deadlines.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
regulatory applicationsapplication submissiondocument researchapplication monitoringadministrative licensing
Soft Skills
communicationorganizational skillsattention to detailtime management
Certifications
Bachelor's Degree