Senior Director, Commercial Supply Chain

Mineralys Therapeutics · United States · $180,000–$200,000 (stated in the posting)

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“Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone.  Its initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor.  Mineralys is headquartered in Radnor, Pennsylvania. For more information, please visit https://mineralystx.com. Follow Mineralys on LinkedIn, Twitter and Bluesky”

Mineralys is a fully remote company.

Position Summary

The Senior Director Commercial Manufacturing will be responsible for providing technical and organizational leadership, project management and oversight of commercial drug product and API manufacturing activities at all contract manufacturers to support scale-up, validation, launch, and continued supply of commercial products and samples needed by the commercial organization.

Key Responsibilities

  1. Head the Commercial Manufacturing function.
  2. Manufactures drug products and API on-time and on-budget to meet forecasted sales volumes.
  3. Participates on the Mineralys Sales and Operations Planning Team to review actual sales/sample distribution and revises drug product and API forecasts accordingly.
  4. Provides forecast updates to all CMOs in accordance with contract requirements.
  5. Provides monthly production and inventory reports from all CMOs to Mineralys Finance for monthly close.
  6. Establishes and oversees commercial manufacturing strategies and operational plans across a portfolio of projects and ensures that they are aligned with the strategic and operational objectives of other functions, and of the company.
  7. Participates in the selection and qualification of third-party suppliers for commercial manufacturing.
  8. Oversees commercial manufacturing operations at third party service providers in a 100% outsourced business model.
  9. Prepares supporting documentation for global regulatory filings and provides technical support for responses to Health Authority comments and inquiries to support commercial marketing applications.
  10. As a subject matter expert (SME) in Drug Product Manufacturing, be a key partner to the Drug Substance, Drug Product, and Analytical Development functions and represent the Commercial Manufacturing function on the CMC Team.
  11. Collaborate with Quality Assurance and Regulatory Affairs to assure compliance with applicable GxP and global regulatory requirements.
  12. Ensure budget, schedules, and performance requirements are met.
  13. May hire, mentor, and develop staff according to the future needs of a growing company.

Education & Experience

Travel

This position is eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level.

US Salary Range:  $180,000-$200,000

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