Senior Regulatory CMC Lead

Solve IT Strategies, Inc.
  • Boston, MA
  • Instant Apply
30+ days ago

Job Description

Primary Responsibilities

1. Global Regulatory CMC Strategy

  • Lead and drive the global Regulatory CMC strategy for biologic ADC programs.
  • Provide strategic guidance for global MAA/BLA preparation and submission activities.
  • Ensure alignment of CMC regulatory strategies with overall development and commercialization objectives.
  • Anticipate regulatory risks and propose mitigation strategies.

2 Regulatory Submission Leadership

  • Lead the CMC aspects of global MAA and/or BLA.
  • Review and support preparation / finalization of Module 3.
  • Ensure consistency, scientific robustness, and regulatory compliance of submission content.
  • Support responses to health authority questions and deficiency letters.

3 Health Authority Interaction Support

  • Lead preparation for FDA, EMA, and other global agency interactions on CMC topics.
  • Review briefing package development and meeting preparation.
  • Provide strategic input on regulatory positioning and negotiation approaches.

4 Cross-Functional Leadership

  • Operate effectively in a global matrix environment.
  • Coordinate cross-functional contributors and external partners where relevant.
  • Facilitate alignment between technical, regulatory, and program objectives.
  • Determine timelines and deliverables across multiple stakeholders.

3.5 Regulatory Intelligence and Compliance

  • Maintain awareness of applicable ICH, FDA, EMA, and international regulatory guidelines related to biologics and ADC products.
  • Ensure compliance with global regulatory expectations for Module 3.

Education and Required Skills

Mandatory Experience

  • Minimum 10 years of experience in Regulatory Affairs CMC within the biotechnology and/or pharmaceutical industry.
  • Proven hands-on experience leading Module 3 of biologic MAA and/or BLA submissions.
  • Strong expertise in biologics.
  • Understanding of ICH, FDA, and EMA regulatory requirements applicable to Module 3.
  • Demonstrated experience defining and implementing global regulatory strategies.

Technical and Professional Competencies

  • Strong strategic thinking and decision-making capabilities.
  • Excellent critical thinking and problem-solving skills.
  • Ability to prioritize multiple projects and competing timelines.
  • Strong stakeholder management and communication skills.
  • Experience working collaboratively in cross-functional and international teams.
  • Pragmatic, scientifically driven, organized, and solution-oriented mindset.

Travel and Location

  • Max 10% to Boston office or Headquarters in Paris (France)
  • Flexible for this to be Boston-office based, remote East-coast (USA) or hybrid.

Numbers & Facts

LocationBoston, MA

Skills

  • Biotech and Pharmaceuticalunmatched
  • Communication Skillsunmatched
  • Cross-Functionalunmatched
  • Establish Prioritiesunmatched
  • FDA (Food and Drug Administration)unmatched
  • FDA Requirementsunmatched
  • ICH Regulationsunmatched
  • Leadershipunmatched
  • Maintain Complianceunmatched
  • Marketing Authorization Application (MAA)unmatched
  • Multitaskingunmatched
  • Negotiation Skillsunmatched
  • Organizational Skillsunmatched
  • Policy Implementationunmatched
  • Presentation/Verbal Skillsunmatched
  • Problem Solving Skillsunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Regulatory Submissionsunmatched
  • Risk Managementunmatched

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