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Job Details

Director MSAT

  2025-09-26     EPM scientific     Houston,TX  
Description:

Director of Manufacturing Science & Technology (MSAT)

📍 Location: Houston, TX | On-site
🕒 Full-time | Executive Leadership Role

Summary

This industry-leading, people-first pharmaceutical company is seeking a Director of Manufacturing Science & Technology (MSAT) to lead transformative efforts in optimizing manufacturing processes and scaling innovative drug products. This role is central to ensuring technical excellence, regulatory compliance, and operational efficiency across clinical and commercial manufacturing. Join a mission-driven organization that's revolutionizing healthcare by making high-quality, affordable medication accessible to all.

Key Responsibilities

  • Lead initiatives to optimize manufacturing processes, reduce waste, and improve product quality across sterile and non-sterile platforms.
  • Oversee technology transfer, process validation, and scale-up activities, ensuring seamless transition from development to production.
  • Provide technical support for batch execution, deviation management, and GMP compliance.
  • Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs, and Supply Chain to align manufacturing strategies.
  • Drive continuous improvement through innovation, risk assessment, and adoption of emerging technologies.
  • Mentor and manage a high-performing team, fostering collaboration, accountability, and growth.
  • Demonstrate expertise in process development, aseptic techniques, and regulatory standards, using data-driven methods for problem-solving and optimization.

Qualifications

  • Advanced degree in Engineering, Pharmaceutical Sciences, or related field (Master's or Ph.D. preferred).
  • Minimum 10 years of experience in pharmaceutical manufacturing, with at least 3 years in a leadership role.
  • Strong background in sterile & non-sterile manufacturing and technology transfer.
  • Proven track record of driving process improvements and managing cross-functional projects.
  • Deep understanding of GMP, regulatory guidelines, and validation protocols.
  • Excellent leadership, communication, and organizational skills.
  • Experience with project management tools and methodologies.

Benefits

  • Offers a strong and comprehensive benefits package to support your health and well-being, including medical, dental, and vision coverage, paid time off, 401(k) matching, wellness perks, and more.


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