Gra Cmc Specialist

Century Center

Plan and monitor regulatory affairs activities
Acquire necessary permits and approvals
Maintain regulatory system data entry
The role involves planning and directing regulatory affairs to ensure the organization holds all necessary permits and licenses for business operations

Job Summary

  • The role involves planning and directing regulatory affairs to ensure the organization holds all necessary permits and licenses for business operations.
  • Candidates will be responsible for acquiring permits, monitoring regulatory developments, and representing the company before legislative or industry standards agencies.
  • CSL Behring is a global biotherapeutics leader driven by a promise to save lives through innovative therapies in immunology, hematology, and other therapeutic areas.

Matching Summary

The role involves planning and directing regulatory affairs to ensure the organization holds all necessary permits and licenses for business operations.

Skills & Requirements

Must-have

  • Plan and monitor regulatory affairs activities
  • Acquire necessary permits and approvals
  • Maintain regulatory system data entry
  • Represent organization before regulatory agencies

Nice-to-have

  • Establish positive relationships with government agencies
  • Advise management on regulatory impacts
  • Collaborate with legal counsel and consultants

Key Requirements

  • Bachelor degree in Life Science or Business
  • 3+ years regulatory experience in pharmaceutical industry
  • Biologics Regulatory experience preferred
  • Advanced degree (PhD, MD, MBA) an advantage

Work Rights

Not specified

Tailored Resume

Cover Letter