Overview
The Bio/Chemical Engineer will support the design, optimization, and scale-up of biopharmaceutical manufacturing processes.
This role focuses on developing robust upstream and downstream operations to ensure consistent product quality and process efficiency in a GMP environment.
Responsibilities
Design and execute laboratory and pilot-scale experiments to support process development and characterization.
Optimize bioreactor and purification operations to improve yield, productivity, and scalability.
Collaborate with cross-functional teams including Analytical Development, Quality, and Manufacturing.
Analyze experimental data to support process understanding, robustness, and control strategies.
Contribute to technology transfer activities from development to clinical and commercial manufacturing sites.
Prepare technical reports, risk assessments, and documentation to support regulatory submissions.
Support troubleshooting of process-related issues in manufacturing as needed.
Qualifications
Bachelor's, Master's, or Ph.D. in Chemical Engineering, Biochemical Engineering, or related field.
2–6 years of relevant experience in biopharmaceutical process development or manufacturing.
Strong understanding of bioreactor operations, mass transfer, and purification principles.
Experience with statistical data analysis tools (e.g., JMP, Minitab) preferred.
Excellent communication, problem-solving, and documentation skills.
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