Remote Global Regulatory Labeling Operations Specialist

Parexel

Olympia (WA)

Remote

USD 90,000 - 130,000

Full time

9 days ago
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Benefits offered by this job

Health, Vision & Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending & Health Savings
Work/Life Balance
401(k) with Company match
Pet Insurance

Job summary

Parexel is seeking a Global Labeling Specialist (Operations) to join our team in a remote capacity. You will support labeling operations, regulatory compliance, and governance across regions, coordinating documents and ensuring timely updates.

Ideal candidates have 3+ years in pharma labeling, strong collaboration skills, and a solid understanding of global labeling requirements. This role offers growth in regulatory affairs and clinical development with a global footprint.

Qualifications

  • Expertise in regulatory labeling operations and document management systems.
  • Experience in pharmaceutical/biotech regulatory environments with global labeling.
  • Strong cross-functional collaboration and clear communication with regulatory teams.
  • Attention to detail in managing regulatory labeling documents.
  • Familiarity with regulatory tracking systems and change management.

Responsibilities

  • Coordinate labeling operations and regulatory-compliant documents across regions.
  • Maintain version control and track labeling in EDMS and regulatory systems.
  • Support CDS, USPI, EU product information and other labeling deliverables.
  • Collaborate with Regulatory, Operations, and regional leads on changes.
  • Provide training on labeling process requirements and governance standards.

Job description

Parexel is seeking a Global Labeling Specialist (Operations) to join our team in a remote capacity. You will support labeling operations, regulatory compliance, and governance across regions, coordinating documents and ensuring timely updates.

Ideal candidates have 3+ years in pharma labeling, strong collaboration skills, and a solid understanding of global labeling requirements. This role offers growth in regulatory affairs and clinical development with a global footprint.

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