Daniel Suero
Tampa,Florida
Summary
Experienced biopharmaceutical team leader with a proven track record driving cell therapy manufacturing operations at Bristol-Myers Squibb. Skilled at supervising cross-functional teams, ensuring compliance with GMP regulations, and maintaining data integrity through integrated manufacturing systems (IMS/MES/LIMS). Adept at coordinating production schedules, executing batch records, and resolving deviations to support timely delivery of life-Experienced biopharmaceutical team leader with a proven track record driving cell therapy manufacturing operations at Bristol-Myers Squibb. Skilled at supervising cross-functional teams, ensuring compliance with GMP regulations, and maintaining data integrity through integrated manufacturing systems (IMS/MES/LIMS). Adept at coordinating production schedules, executing batch records, and resolving deviations to support timely delivery of life-saving therapies. Recognized for optimizing workflows, mentoring staff, and collaborating with Quality and Engineering to implement process improvements. Seeking to leverage leadership, systems expertise, and operational excellence in a Cell Therapy IMS Analyst role.
saving therapies. Recognized for optimizing workflows, mentoring staff, and collaborating with Quality and Engineering to implement process improvements. Seeking to leverage leadership, systems expertise, and operational excellence in a Cell Therapy IMS Analyst role.
Overview
2026
2026
years of professional experience
Work History
Cell Therapy Team Leader
Bristol Myers Squibb
2020 - 06.2025
- Operated and maintained GMP-regulated manufacturing equipment to support production of advanced therapies, including cell therapy products.
- Performed in-process monitoring, batch documentation, and deviation reporting to ensure compliance with FDA, cGMP, and company quality standards.
- Collaborated with cross-functional teams—including Quality, Engineering, and Supply Chain—to resolve issues and ensure continuous operations.
- Executed batch records, electronic logbooks, and inventory transactions accurately within integrated manufacturing systems (IMS/MES/LIMS).
- Supported process improvement initiatives by identifying bottlenecks, performing root cause analysis, and recommending system or workflow enhancements.
- Trained and mentored new technicians on standard operating procedures (SOPs), safety protocols, and electronic system usage.
- Ensured readiness for internal and external audits by maintaining meticulous documentation and adhering strictly to validated processes.
Education
Associate of Arts - Liberal Arts in Business
Middlesex County College
Edison, NJ05.2019
Skills
GMP compliance, manufacturing execution systems (MES/IMS), data integrity, deviation management, batch record review, inventory control, cross-functional collaboration, and regulatory audit readiness
Timeline
Cell Therapy Team Leader
Bristol Myers Squibb
2020 - 06.2025
Associate of Arts - Liberal Arts in Business
Middlesex County College
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