Head of Manufacturing Science and Technology; MSAT
Listed on 2025-12-20
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Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing Engineer, Validation Engineer
Head of Manufacturing Science and Technology (MSAT)
Location:
Oklahoma City Metropolitan Area
Biopharmaceuticals | Large Molecules | GMP Manufacturing
About the RoleA leading biopharmaceutical manufacturing organization is seeking an experienced Head of Manufacturing Science & Technology (MST) to lead and develop its MST function. This role is critical to supporting GMP manufacturing operations, driving process excellence, and ensuring successful technology transfer and scale-up for large molecule programs.
The successful candidate will provide technical leadership across production support, process optimization, and regulatory readiness, while building and mentoring a high‑performing MST team.
Key Responsibilities- Develop and execute annual MST plans aligned with overall business strategy, operational goals, and regulatory requirements
- Lead and manage the MST team, providing technical oversight and day‑to‑day support to GMP manufacturing operations
- Serve as the technical escalation point for manufacturing challenges, ensuring timely root‑cause analysis and resolution
- Drive process development, optimization, and continuous improvement to enhance process robustness, efficiency, and compliance
- Lead technology transfer and scale‑up activities, ensuring reproducibility and successful integration into commercial manufacturing
- Support internal and external audits and regulatory inspections, ensuring processes and documentation meet GMP standards
- Establish, optimize, and maintain laboratory systems, procedures, and quality standards to ensure reliable and compliant data generation
- Develop, coach, and mentor MST team members to strengthen technical capability, leadership, and overall performance
- Master’s degree or higher in Biotechnology, Pharmaceutical Sciences, Chemical Engineering, or a related discipline
- Minimum of 10 years’ experience in the biopharmaceutical industry, with at least 5 years in a people management role
- Strong expertise in large molecule development, technology transfer, process optimization, and GMP manufacturing
- Proven ability to troubleshoot complex technical issues in a production environment
- Excellent communication, problem‑solving, and cross‑functional collaboration skills
- Strong leadership skills with a demonstrated ability to develop technical teams
- Fluent in English (written and spoken)
- Background within a CDMO or contract manufacturing environment
- Familiarity with U.S. FDA and EU regulatory expectations
This is a senior leadership opportunity to shape manufacturing science and technology strategy within a growing biopharmaceutical operation, offering significant influence over process performance, regulatory success, and team development.
Seniority level- Director
- Full‑time
- Manufacturing and Science
- Pharmaceutical Manufacturing and Biotechnology Research
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