Senior Regulatory CMC Lead

Solve IT Strategies, Inc.

Senior Regulatory CMC Lead

Boston, MA
Full Time
Paid
  • Responsibilities

    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.