The role requires a senior industry professional to oversee the successful completion of a large-scale biopharmaceutical greenfield project currently in the commissioning phase
Job Summary
The role requires a senior industry professional to oversee the successful completion of a large-scale biopharmaceutical greenfield project currently in the commissioning phase.
Candidates must demonstrate extensive experience managing complex CQV activities within major capital investment projects exceeding USD 500 million.
The position involves leading multidisciplinary teams through peak commissioning and qualification activities while ensuring alignment across all stakeholders.
Matching Summary
Match Score: 85
The role requires a senior industry professional to oversee the successful completion of a large-scale biopharmaceutical greenfield project currently in the commissioning phase.
Skills & Requirements
Must-have
30 years of CQV experience
Large-scale greenfield project leadership
GMP and FDA regulatory compliance
Cross-functional stakeholder management
Commissioning and validation execution
Nice-to-have
Experience with biologics or cell therapy
Client-side CQV lead background
Familiarity with digital CQV systems
Integrated project delivery models
Sterile manufacturing facility experience
Key Requirements
Minimum 30 years of CQV experience
Proven track record on mega projects over $500M
Deep understanding of GMP, FDA, and EMA regulations