Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Grifols

Plasma Regulatory Affairs Associate

Grifols

Plasma Regulatory Affairs Associate managing regulatory applications and ensuring FDA compliance for plasma collection in North America. Collaborating with internal teams and external regulatory agencies for timely submissions and updates.

Posted 7/28/2026full-timeRTP • North Carolina • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in preparing regulatory applications and managing submission processes within the pharmaceutical or blood industry. Proficient in utilizing Microsoft Office and Adobe PDF for documentation and communication.

Highest-signal resume keywords
Regulatory Application PreparationPharmaceutical Industry ExperiencePlasma Collection KnowledgeMicrosoft Office ProficiencyAdobe PDF Experience

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Regulatory Application PreparationApplication Submission MonitoringDocument Research and CompletionCover Letter PreparationSummary Writing
Soft Skills
CommunicationOrganizational SkillsAttention to Detail
Tools & Technologies
Microsoft OfficeAdobe PDF
Industry Keywords
Pharmaceutical IndustryRegulated FieldTechnical ExperienceLicensing Activities

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
  • Medical insurance
  • Paid vacation
  • Retirement plan
  • Opportunities for professional development
  • Flexible working hours