Head of MSAT
Job in
Oklahoma City, Oklahoma County, Oklahoma, 73116, USA
Listed on 2026-01-22
Listing for:
BioTalent
Full Time
position Listed on 2026-01-22
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing Engineer
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 ResponsibilitiesAs 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
- 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
- Experience with in a CDMO environment
- Knowledge of FDA and EU regulatory requirements
Please reach out to for more information.
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