This role serves as the enterprise-wide single point of ownership for the Drug Product aspect of the Global Manufacturing Standardization Strategy
Job Summary
This role serves as the enterprise-wide single point of ownership for the Drug Product aspect of the Global Manufacturing Standardization Strategy.
The incumbent is accountable for defining the global strategy and roadmap to ensure cross-site equivalency and unparalleled efficiencies in DP fleet systems.
Roche offers a culture that encourages personal expression, open dialogue, and genuine connections where every voice matters.
Matching Summary
This role serves as the enterprise-wide single point of ownership for the Drug Product aspect of the Global Manufacturing Standardization Strategy.
Skills & Requirements
Must-have
Master's degree in Engineering or Life Sciences
15 years pharmaceutical industry experience
Drug Product manufacturing lifecycle management
GMP and ICH Q10/Q12 regulatory compliance
Global multi-site operations leadership
Nice-to-have
PhD in related technical field
Experience with Pre-Approval Inspections
Change management in regulated environments
Cross-functional alignment across geographies
Key Requirements
Master's degree required; PhD strongly preferred
Minimum 15 years of experience in pharma/biotech
Expertise in GMP, Quality Systems, and ICH guidelines
Proven track record in managing complex equipment lifecycle