Senior Director, External Manufacturing

Amylyx PharmaceuticalsCambridge, MA
$245,000 - $276,000Remote

About The Position

The Senior Director, External Manufacturing is a critical leadership role responsible for shaping and executing the external manufacturing strategy across clinical and future commercial programs. This individual will lead a global network of CDMO partners supporting a diverse and growing portfolio spanning peptides, oligonucleotides, and small molecules. As Amylyx advances toward commercialization and expands its global manufacturing footprint, this role will be instrumental in ensuring supply continuity, operational readiness, and long-term scalability. The Senior Director will partner cross-functionally to enable successful product launches, manage increasing manufacturing complexity, and build the infrastructure needed to support future growth and global expansion.

Requirements

  • Bachelor’s degree in engineering, life sciences, or related field; advanced degree preferred
  • ~15+ years of experience in pharmaceutical or biotechnology manufacturing, including significant external manufacturing leadership
  • Proven track record managing CDMOs across clinical and commercial supply environments
  • Deep understanding of cGMP regulations, global manufacturing requirements, and regulatory expectations
  • Experience in manufacturing strategy, technology transfer, and commercialization activities
  • Demonstrated ability to lead in complex, multi-program environments and drive cross-functional alignment
  • Strong leadership, communication, and stakeholder management skills
  • Prior experience supporting commercial product launches, conducting RFPs, negotiating supply agreements, and managing high value budgets
  • Experience across multiple supply nodes (API, Drug Product, Packaging, Device)
  • Ability to travel domestically and internationally ~10%

Nice To Haves

  • Experience across multiple modalities (small molecule, peptide, oligonucleotide)
  • A track record of process scale-up, validation and continuous improvement

Responsibilities

  • Provide strategic leadership and oversight of external manufacturing across clinical development and commercial supply
  • Establish and govern CDMO partnerships to ensure strong performance, accountability, and alignment with program objectives
  • Define and execute manufacturing strategies to support technology transfer, scale-up, commercialization, and lifecycle management
  • Establish supplier performance metrics and business review process
  • Mentor and build a team of relationship owners responsible for leading the internal supplier relationship teams and serving as the supplier point of contact
  • Ensure supply continuity through proactive risk identification, mitigation planning, and issue escalation across external partners
  • Oversee technology transfer, manufacturing execution, and process performance across a global network of external sites
  • Support commercial launch readiness, including validation, supply planning, and inspection preparedness
  • Partner cross-functionally with Finance, Legal, CMC, Quality, and Supply Chain to drive aligned execution
  • Build scalable, robust external manufacturing infrastructure, operating models, and governance frameworks to support organizational growth

Benefits

  • health insurance coverage
  • state tax regulations
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service