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Head of MSAT

Job in Oklahoma City, Oklahoma County, Oklahoma, 73116, USA
Listing for: BioTalent
Full Time position
Listed on 2026-01-22
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below

Bio Talent are seeking a skilled and experienced Head of MSAT to lead the Manufacturing Science & Technology function at our CDMO Client. This senior leadership role is central to biologics manufacturing, focusing on strategic direction, technical excellence, and operational support.

If you have a strong background in large‑molecule process technologies, thrive in GMP environments, and are motivated to drive continuous improvement, this position offers an opportunity to make a significant impact.

Key Responsibilities

As Head of MSAT, you will be responsible for ensuring process robustness, operational continuity, and technical compliance across all manufacturing activities, including:

  • Developing annual MSAT plans aligned with organisational strategy and operational goals
  • Leading the MSAT team to deliver high‑quality technical support to production
  • Overseeing process technology development to enhance capability, efficiency, and compliance
  • Troubleshooting and resolving complex production issues to ensure stable operation
  • Managing technology transfer and scale‑up activities to ensure reproducible and robust processes
  • Supporting GMP audits and inspections and ensuring documentation meets regulatory expectations
  • Establishing and optimising laboratory systems, procedures, and quality standards
  • Providing leadership, coaching, and development to build technical capability across the MSAT team
Requirements
  • Master’s degree or higher in Biotechnology, Pharmaceuticals, Chemical Engineering, or a related discipline
  • Minimum of 10 years’ experience in the biopharmaceutical industry, including at least 5 years in team leadership or management
  • Strong expertise in large‑molecule development, tech transfer, process optimisation, and GMP compliance
  • Excellent analytical, problem‑solving, communication, and collaboration skills
  • Demonstrated leadership ability and a track record of developing high‑performing teams
  • Proficiency in written and spoken English
Preferred Experience
  • Experience with in a CDMO environment
  • Knowledge of FDA and EU regulatory requirements

Please reach out to  for more information.

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