This role involves supporting technology transfer and process validation activities for biopharmaceutical drug product manufacturing, specifically sterile injectables
Job Summary
This role involves supporting technology transfer and process validation activities for biopharmaceutical drug product manufacturing, specifically sterile injectables.
You will prepare and maintain technical, validation, and regulatory documentation in compliance with GMP and regulatory requirements, and collaborate with cross-functional partners.
Pfizer offers a supportive environment with opportunities for career enhancement, professional development, and a strong focus on integrity, quality, and respect for people.
Matching Summary
This role involves supporting technology transfer and process validation activities for biopharmaceutical drug product manufacturing, specifically sterile injectables.
Skills & Requirements
Must-have
Technology transfer
Process validation
GMP and regulatory compliance
Biopharmaceutical drug product manufacturing
Sterile injectables
Scientific and technical support
Nice-to-have
Ownership and accountability
Analytical thinking
Problem-solving mindset
Dynamic manufacturing environment
Cross-functional collaboration
Willingness to learn and adapt
Key Requirements
University degree (VSS / 300 ECTS)
Experience in technical services, technology transfer, process validation, or process support
Working knowledge of GMP and regulatory expectations