Reviews and approves pharmaceutical batch records, GMP documentation, cleaning records, deviations, change controls, investigations, and quality assessments. Performs API disposition, monitors quality metrics and trends, supports annual product reviews, inspection readiness, validated systems, regulatory submissions, and continuous improvement. Requires pharmaceutical quality experience, GMP knowledge, strong communication, and teamwork.

Lead Oncology Medical Affairs for Singapore and the Philippines by executing field medical strategies, engaging external experts, planning advisory boards and congress representation, supporting Pfizer-sponsored research, coordinating cross-functional medical projects, ensuring compliance, delivering scientific training, capturing medical insights, and supporting Category Medical Lead on strategy and capability building.

Leads external supply operations for Pfizer’s portfolio of contract manufacturers and partners primarily in Japan. Responsibilities include CMO relationship and performance management, P&L ownership, supply and manufacturing planning, quality and compliance oversight, cost reduction, product transfers, new product introductions, investigations, business continuity, and cross-functional virtual site leadership. Requires strong pharmaceutical manufacturing, supply chain, regulatory, negotiation, and stakeholder-management expertise, plus Japanese and English fluency. Travel is 20–25%, primarily across Japan.