Course Overview

Every batch, every audit, and every dollar of margin hinges on how seamlessly your workforce executes the end‑to‑end bioprocess. This course turns new and seasoned employees into cross functional thinkers who understand the critical hand offs from upstream through downstream to fill finish, driving operational excellence across the entire bioprocess lifecycle.

What Your Team Will Learn

• Full-line process understanding – see, touch, and map every major unit operation inside a GMP-simulated environment.
• Regulatory red-flags – identify the hidden compliance traps that lead to warning letters, recalls, and costly CAPAs.
• Quality culture mindset – link each SOP step to product safety and patient outcomes, cementing right-first-time behaviours.

Who Should Attend

This course is designed for individuals across the biopharmaceutical industry who seek a fundamental understanding of bioprocessing, including:

• Operators and technicians supporting day-to-day bioprocess operations
• Engineers involved in upstream, downstream, or overall process development and manufacturing
• QA/QC associates ensuring quality, compliance, and product integrity across process stages
• Managers overseeing production, technical teams, or facility operations
• Clinical trial personnel working with investigational biologics or supporting manufacturing-readiness
• Supply chain professionals responsible for materials, logistics, or production planning
• Anyone working directly or indirectly in the manufacturing and development of biopharmaceutical products