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Senior Director, External Manufacturing

Job in New York, New York County, New York, 10261, USA
Listing for: Ladders
Full Time position
Listed on 2026-10-16
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 270000 - 290000 USD Yearly USD 270000.00 290000.00 YEAR
Job Description & How to Apply Below
Location: New York

For our client, we are seeking a Senior Director, External Manufacturing to join the team of a leader in the Pharmaceuticals & Biotech space.

This leader will own the external manufacturing strategy and day-to-day partnership management for a portfolio of clinical and commercial programs. The role is focused on building strong CDMO governance, ensuring manufacturing readiness, and driving reliable supply across a global network. It will partner closely with Quality, Technical Operations, Regulatory, and cross-functional teams to support technology transfer, validation, and compliance outcomes.

Location:

New York, NY - US based candidates only, no visa sponsorship available

Compensation: $270,000 - $290,000 annually

Responsibilities
  • Own relationships with CDMOs, including governance, performance management, and regular business reviews
  • Oversee external drug manufacturing operations for clinical and commercial programs
  • Lead selection and integration of manufacturing partners in collaboration with cross-functional teams
  • Ensure effective technology transfer and validation processes with technical leads
  • Drive CDMO performance and manufacturing readiness across the network
  • Collaborate with Quality teams to maintain compliance with cGMP standards
  • Monitor and resolve operational risks related to production plans and schedules
  • Support regulatory filings and ensure manufacturing partner readiness
Qualifications
  • Bachelor's degree in chemistry, chemical engineering, biochemistry, pharmaceutical sciences, or a related field; advanced degree or MBA preferred
  • 15+ years of pharmaceutical or biotechnology manufacturing experience, including leadership in outsourcing and global partnerships
  • Deep experience in small molecule API and oral solid dose manufacturing required
  • Experience with biologics and sterile drug products preferred
  • Demonstrated ability to manage international CDMOs across multiple regions and time zones
Benefits
  • Equity offering as part of the compensation package
  • Annual target bonuses based on performance
  • Comprehensive benefits program including health, wellness, and retirement options

Our client is an equal opportunity employer. We encourage you to apply even if you don't meet every qualification-your background could be exactly what this team needs.

Position Requirements
10+ Years work experience
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