Job Description
This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
What You Will Achieve
In this role, you will:
Evaluate and review commercial drug batches to ensure compliance with established specifications.
Ensuring Zero Defect Technology transfer for new product transfers into site.
Quality Support and review of Scale-up, pilot bio batches and exhibit beaches to meet regulatory expectations.
Reviews of Process validation protocols and reports to meet regulatory expectations.
Review of Optimization Report /Technology Transfer Report, Analytical Data Sheet and Stability Data.
Responsible to manage New Product Introduction (NPI) projects.
Review and approval of Project validation protocols, QRM's, Cleaning validation protocols and reports, process validation protocols & reports, Filter validation protoc...
What You Will Achieve
In this role, you will:
Evaluate and review commercial drug batches to ensure compliance with established specifications.
Ensuring Zero Defect Technology transfer for new product transfers into site.
Quality Support and review of Scale-up, pilot bio batches and exhibit beaches to meet regulatory expectations.
Reviews of Process validation protocols and reports to meet regulatory expectations.
Review of Optimization Report /Technology Transfer Report, Analytical Data Sheet and Stability Data.
Responsible to manage New Product Introduction (NPI) projects.
Review and approval of Project validation protocols, QRM's, Cleaning validation protocols and reports, process validation protocols & reports, Filter validation protoc...
Ready to Apply?
Submit your application today and join our talented team at Pfizer.
Submit ApplicationJob Details
- Location Visakhapatnam, Andhra Pradesh
- Job Type Full-time
- Category Operations Specialties Managers
- Posted Date June 12, 2026
- Application Deadline July 22, 2026