This temporary ESI role sits in the Pharmaceutical Supply & Engineering Sciences (PSES) organization and will be based in Shanghai, working closely with the global PSES and DP development teams
Job Summary
This temporary ESI role sits in the Pharmaceutical Supply & Engineering Sciences (PSES) organization and will be based in Shanghai, working closely with the global PSES and DP development teams.
The role’s primary focus is the day-to-day management, coordination and technical oversight of clinical manufacturing activities at that supplier, ensuring right‑first‑time introductions, robust tech transfers and ongoing supplier performance aligned with global GMP and project timelines.
Serve as the single PSES point of contact and the primary technical lead for our main supplier in China, managing the supplier relationship and acting as the interface between the supplier and internal DP development, QA, regulatory and supply chain teams.
Matching Summary
This temporary ESI role sits in the Pharmaceutical Supply & Engineering Sciences (PSES) organization and will be based in Shanghai, working closely with the global PSES and DP development teams.
Skills & Requirements
Must-have
GMP-regulated pharmaceutical development
clinical drug product manufacturing
supplier relationship management
technical oversight of manufacturing
process validation
risk management
Nice-to-have
innovative technologies
process analytical technologies
international cross-functional teams
Key Requirements
MSc or PhD in chemistry, pharmaceutical sciences, (bio)chemical or mechanical engineering
Minimum of 2 years’ experience in GMP-regulated pharmaceutical development/engineering
Proven experience managing an external manufacturing partner in China