Senior Scientist, Regulatory Cmc Biologics

Merck Merck · Pharma · PA

This role is for a Senior Scientist in Regulatory CMC Biologics at Merck. The primary focus is on providing CMC Regulatory leadership for biological projects, ensuring the delivery of regulatory milestones throughout product development and post-approval life cycles. Responsibilities include developing and executing global CMC regulatory strategies, managing CMC documentation (IND/IMPD, BLA/MAA, variations), and responding to health authority questions, all while maintaining compliance. The role requires a B.S. in a science/engineering field and 5 years of relevant experience in Regulatory CMC for biologicals.

What you'd actually do

  1. Serve as a Regulatory CMC Project Lead and provide CMC Regulatory leadership within Regulatory and on cross-functional teams for the assigned biological projects.
  2. Be accountable for the delivery of all regulatory milestones through product development and / or post approval life cycle.
  3. Ensure development of robust CMC regulatory strategies for assigned projects.
  4. Be accountable for the execution of global product regulatory strategy(ies) by robust assessment of global regulatory CMC requirements and identification of potential risks.
  5. Manage execution of CMC documentation including IND/IMPD, original BLA/MAA, or Post approval / variations, agency background packages and responses to health authority questions per established business processes and systems.

Skills

Required

  • Business Processes
  • CMC Documentation
  • CMC Strategy
  • Detail-Oriented
  • Document Coordination
  • Drug Product Development
  • Interpersonal Relationships
  • Pharmaceutical Products
  • Regulatory CMC
  • Regulatory Communications
  • Regulatory Compliance
  • Regulatory Interpretation
  • Regulatory Project Management
  • Regulatory Strategy Development
  • Writing Technical Documents

Nice to have

  • CMC Biologics

What the JD emphasized

  • Regulatory CMC
  • biological projects
  • CMC regulatory strategies
  • global regulatory CMC requirements
  • CMC documentation
  • health authority questions
  • compliance