Module 1: The Cleanroom Reality & Industry Mindset (Live 2.5-Hour Digital Masterclass via Teams)

Time: May 12th at 3.00-5.30 pm

• The Disconnect: Why academic lab experience is often viewed as a liability in a commercial Grade B/C cleanroom.
• GMP Fundamentals: Introduction to EMA/FDA regulations and the financial/legal weight of Good Manufacturing Practice.
• Shop-Floor Logic: Cleanroom classifications, strict aseptic gowning protocols, and the operator as the primary contamination risk.
• The Golden Rule: Introduction to ALCOA++ principles. Learning that in the pharma industry, "If it isn't documented, legally, it did not happen."

Module 2: Practical Application & The ATS CV Pivot (Live 2.5-Hour Digital Masterclass via Teams)

Time: May 19th at 3.00-5.30 pm

• When Things Go Wrong: A high-level introduction to Deviation Management and Root Cause Analysis (The 5 Whys, Ishikawa).
• What is a CAPA? Understanding Corrective and Preventive Actions—the most critical vocabulary word for European pharma interviews.
• CV Optimization for Pharma: How to stop listing "academic lab chores" and start translating university experience into industry-recognized keywords (e.g., swapping "buffer preparation" for "compliance-driven material handling").

Module 3: The "Industry-Ready" Assignment (Independent Work)

• The Deliverable: Following Module 2, participants will take their current academic CV and rewrite the top half using the GxP Bridge industry framework.
• The Feedback: Participants submit their revised CV profiles, and GxP Bridge provides high-level feedback on their new industry terminology, ensuring they are ready to apply for QA, QC, and Bioprocess Engineering roles.