

Results-driven Chemical Engineer, Chemist, and Biotechnology Specialist (M.Sc.) with 5+ years of experience in biotechnology and pharmaceutical manufacturing within GMP-regulated environments. Proven track record of delivering operational improvements, including a 30% reduction in WFI consumption, a 15% reduction in production downtime, and a 5% reduction in energy usage through process optimization initiatives. Expertise includes downstream processing, recombinant protein manufacturing, Lean Six Sigma, OEE, SAP, and quality systems. During a dedicated professional development period (2022-2026), further advanced technical, digital, language, and business capabilities through continuous learning and ongoing studies in International Trade & Logistics.
Biotechnology manufacturing
Downstream processing
Recombinant protein production
Tangential flow filtration (TFF)
GMP compliance
Validation protocols
Cleaning validation
CIP/SIP validation
Batch record review
Deviation investigation
Process parameter optimization
Continuous improvement
Operational excellence
OEE analysis
Change control
Process improvement
Manufacturing operations
Six sigma methodologies
Production scheduling
Workflow management
Schedule development
ISO standards
Cost reduction strategies
Hand tool proficiency
Quality inspection
Documentation
Complex Problem-solving
Quality assurance
Manufacturing support
Computer skills
Production line work
Cycle counts
Entrepreneurship
Python
Visual code
Ms Office
Power BI
Aspen
Chemcad