Regulatory Affairs - Labeling

Merck Merck · Pharma · Central Bohemian, Czech Republic

This role is responsible for managing and executing labeling operational tasks within the pharmaceutical industry, ensuring compliance with regulatory standards and supporting product launches. It involves serving as a point of contact, processing updates, performing quality checks, and collaborating with cross-functional teams.

What you'd actually do

  1. Serving as the primary labeling operations point of contact for Global, US, and EU Labeling Leads
  2. Receiving, reviewing, and processing labeling operational tasks for Core, US and EU labeling update requests on schedule, ensuring timely resolution of any issues throughout the update cycle while ensuring all labeling deliverables meet regulatory standards and timelines with consistent, high-quality execution
  3. Performing labeling operational tasks (quality checks, verifications, proofreading, creation of labeling documents, including US SPL, and updating trackers)
  4. Providing effective functional oversight in situations where a vendor performs labeling operational tasks
  5. Collaborating with cross-functional teams to prioritize and manage labeling operational support for labeling updates, which may include product launches

Skills

Required

  • Detail-Oriented
  • Labeling Systems
  • Medical Writing
  • Policy Implementation
  • Preventive Action
  • Prioritization
  • Promotional Review
  • Proofreading
  • Regulatory Affairs Management
  • Regulatory Communications
  • Regulatory Compliance Audits
  • Regulatory Labeling

What the JD emphasized

  • regulatory standards
  • labeling operational tasks