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Director, Peptide Process Development

Job in Cambridge, Middlesex County, Massachusetts, 02141, USA
Listing for: Alnylam Pharmaceuticals
Full Time position
Listed on 2026-08-05
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing, Pharmaceutical Science/ Research, Validation Engineer
Job Description & How to Apply Below

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 $ - $

The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).

Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k) with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks.

We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.

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