Jobs at Pfizer

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.

Supports environmental, health, and safety compliance at a manufacturing site through inspections, audits, risk assessments, incident investigations, corrective actions, environmental programs, emergency preparedness, training, documentation, contractor coordination, and regulatory reporting. The role also contributes to facility projects, sustainability initiatives, performance monitoring, and continuous improvement of EHS systems and safety culture.

Manages quality and compliance activities for Pfizer’s external manufacturers, suppliers, and partners. Responsibilities include supplier quality oversight, audits, GMP/GDP compliance assessments, vendor risk management, quality improvement plans, investigations, product quality reviews, stability reports, batch disposition endorsement, quality agreements, and regulatory inspection support. Leads cross-functional virtual teams, supports CMO onboarding and offboarding, drives continuous improvement, and provides quality leadership and performance reporting.

Manages customs compliance and day-to-day customs operations across APAC, ensuring adherence to local regulations, Pfizer policies, GDP/GMP standards, and health authority requirements. Identifies and mitigates customs risks, prevents penalties, oversees brokers and authorities, monitors performance, and drives corrective actions and process improvements. The role also leads regional projects, represents APAC in global forums, and supports compliant movement of pharmaceutical products.

Design, monitor and improve pharmaceutical manufacturing processes to ensure GMP, quality, EHS and data integrity. Lead production campaigns, troubleshoot process issues, develop SOPs, train technicians, drive continuous improvements and support cross-functional investigations and transfers.

The Senior Process Engineer will lead manufacturing campaigns, develop operating instructions, troubleshoot quality issues, ensure adherence to GMP standards, and collaborate with cross-functional teams to improve processes.

Operates automatic and manual chemical process equipment in pharmaceutical manufacturing. Performs material handling, equipment preparation, sampling, dispensing, charging, documentation, and plant monitoring in accordance with cGMP and GxP standards. Troubleshoots routine process deviations, supports quality and safety investigations, coordinates with maintenance and other departments, and ensures accurate, safe, and uninterrupted production under moderate supervision.