Director, Supply Chain

Scorpion Therapeutics

United States

Remote

USD 180,000 - 240,000

Full time

14 days+
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Job summary

Outlook Therapeutics is seeking a Director of Supply Chain & Manufacturing Planning to oversee end-to-end manufacturing strategy for a globally launched ophthalmic product. You will lead production planning, coordinate with CMOs/CROs, and ensure scheduling, logistics, and regulatory submissions are aligned with the product launch.

The role requires 8+ years in pharma supply chain/manufacturing, with a strong background in regulated environments, project management, and cross-functional

Qualifications

  • 8+ years in pharmaceutical manufacturing or supply chain in regulated environments.
  • Experience in project management and cross-functional leadership.

Responsibilities

  • Lead production planning.
  • Collaborate with internal teams and external partners (CMOs/CROs).
  • Oversee scheduling.
  • Manage supply chain risks.
  • Optimize resources.
  • Coordinate logistics.
  • Support regulatory submissions.

Skills

Cross-functional leadership

Education

B.S./M.S./Ph.D. in life sciences or technical field

Tools

Advanced planning software
Lean/Six Sigma
AI/digital tools

Job description

Director of Supply Chain & Manufacturing Planning

responsible for end-to-end commercial manufacturing strategy, supporting global launch of Outlook Therapeutics' FDA-approved ophthalmic product for wet AMD.

Responsibilities
  • lead production planning
  • collaborate with internal teams and external partners (CMOs/CROs)
  • oversee scheduling
  • manage supply chain risks
  • optimize resources
  • coordinate logistics
  • support regulatory submissions
Requirements

B.S./M.S./Ph.D. in life sciences or technical field; 8+ years in pharmaceutical manufacturing or supply chain management, with experience in regulated environments, project management, and cross-functional leadership.

Preferred
  • cold-chain biotech supply chain expertise
  • Lean/Six Sigma knowledge
  • advanced planning software
  • AI/digital tools familiarity
  • risk management
  • international trade experience
High-value
  • focus on biologics
  • ophthalmic drugs
  • post-approval commercial scale-up
  • GxP compliance
  • global logistics
  • cross-functional collaboration with Quality, Operations, and Regulatory teams
Work setup

remote (US-based) with occasional travel to manufacturing sites.

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