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Director, Peptide Process DevelopmentAlnylam PharmaceuticalsCambridge, Massachusetts, United States
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Director, Peptide Process Development

Alnylam Pharmaceuticals
  • US
    Cambridge, Massachusetts, United States
  • US
    Cambridge, Massachusetts, United States

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Director, Peptide Process Development

The Director of Peptide & Peptide-Oligonucleotide Conjugate (POC) Process Development will provide technical leadership for the development, scale-up, and external manufacture of peptide and POC active pharmaceutical ingredients. This role is accountable for advancing robust, scalable, and regulatory-ready processes from early development through clinical and commercial supply. This position requires a balance of hands-on technical expertise, strong CDMO management experience, and cross-functional leadership to deliver peptide and POC processes that are fit for development, manufacture, and future scale. This position is onsite and will be primarily located in Cambridge, MA.

Responsibilities:

  • Lead process development, optimization, scale up, and characterization of peptides and contribute to the development of peptide oligonucleotide conjugate (POC) APIs with internal stakeholders.
  • Serve as the technical lead for peptide and POC processes from development through external GMP manufacture.
  • Evaluate, select, and enable CDMOs; lead process transfer and external manufacturing activities.
  • Author and review technical and regulatory documentation supporting API manufacture and filings.
  • Integrate CMC process activities within TOQ and extended program teams.
  • Contribute to long-term peptide and POC platform strategy and delivery.

Qualifications:

  • PhD in a relevant scientific discipline with 10+ years of industry experience in peptide and/or conjugate process development.
  • Demonstrated expertise in peptide API development, scale up, and process characterization.
  • Experience in process development, optimization, scale-up, and process characterization of peptide-drug conjugates and/or oligonucleotide conjugates.
  • Proven experience leading process transfer and external CDMO-based GMP manufacturing.
  • Experience supporting CMC documentation and regulatory filings.
  • Ability to function as a technical owner within cross-functional program teams.

U.S. Pay Range $197,100.00 - $266,700.00

  • Cambridge, Massachusetts, United States

Sprachkenntnisse

  • English
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