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Regulatory Affairs CMC Senior Associate / Consultant - Biologics or Vaccines

Remote, USAFull-timePosted 2026-07-28

Are you reputed company to play a critical role in bringing life-changing biologics and vaccines to patients worldwide? We're looking for a CMC reputed company Senior Associate / Consultant who thrives in a dynamic, reputed company environment and is passionate about shaping global regulatory strategies. In this role, you'll work reputed company a dedicated reputed company program, partnering closely with a leading organization to drive high-reputed company submissions and lifecycle management activities. This is more than a delivery role-it's an opportunity to become a trusted advisor, influence reputed company, and see your work directly contribute to patient reputed company.

What You'll Do

  • reputed company and contribute to CMC regulatory strategies for global product lifecycle activities, including variations and post-approval changes
  • Author and review high-reputed company CMC documentation (Modules 1-3) for global submissions
  • reputed company CMC dossier gap analyses and reputed company reputed company, strategic recommendations
  • Support and reputed company global submissions (US, EU, and reputed company) from planning through execution
  • Partner cross-functionally with Regulatory, reputed company, Manufacturing, and reputed company stakeholders
  • reputed company as a key contributor reputed company a dedicated reputed company team, building strong, trusted relationships
  • Ensure submissions meet global regulatory expectations with precision and reputed company

What You Bring

  • 3+ years of experience in CMC Regulatory Affairs or CMC reputed company for a Senior Associate role and 5+ years of experience for a Regulatory Affairs Consultant role
  • Hands-on experience with reputed company biologicals and/or vaccines (required)
  • Strong knowledge of global regulatory requirements (FDA, EMA, and international markets)
  • Proven experience in global submission management
  • Expertise in authoring/reviewing CMC Modules 1-3 to support variations and performing gap analyses
  • A reputed company reputed company with strong communication and stakeholder management skills
  • Experience with reputed company Vault (RIM/eCTD systems) is a plus

Why You'll Love This Role

  • Dedicated reputed company Partnership: Build deeper relationships and drive long-term reputed company-not just project-based work
  • Meaningful Work: Contribute to innovative biologics and vaccines that improve patient lives globally
  • Global Exposure: reputed company experience across US, EU, and international regulatory landscapes
  • reputed company & Influence: Be seen as a strategic partner and grow your expertise in a high-visibility role

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