PHARMAFull-time
Associate Manager - Quality Assurance
VIZAG (IN)ONSITEPOSTED: 8/11/2026
PHARMAFull-time
HIRING ORGANIZATIONPFIZERBiopharmaceutical / Healthcare
ROLE DEFINITION & RESPONSIBILITIES
Lead Quality Assurance and oversight for New Product Introduction (NPI) projects and technology transfers at the Vizag facility to ensure Zero Defect site execution.
Review and approve change controls, validation protocols (process, cleaning, filter), project validation reports, PRQs, and Quality Risk Management (QRM) assessments.
Provide QA oversight and data reviews for scale-up, pilot bio batches, exhibit batches, optimization reports, analytical method transfers, and stability data.
Evaluate and review commercial sterile drug batches and production documentation to maintain strict compliance with global regulatory standards and Pfizer quality systems.
Investigate and document QA deviations, evaluate GxP impacts, manage configuration compliance, and escalate quality issues to site leadership.
REQUIRED VERIFIED SKILLS
Quality Assurance
Sterile Injectables
Technology Transfer
Process Validation
Cleaning Validation
Change Control
GxP / cGMP
Quality Risk Management (QRM)
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
Pfizer Inc. is an American multinational pharmaceutical and biotechnology corporation. It is dedicated to the discovery, development, manufacturing, marketing, and sale of medicines and vaccines worldwide. The company focuses on breakthrough science to deliver innovative treatments across various therapeutic areas to improve health outcomes.
TEAM SIZE: 80,000+ employees
INDUSTRY: Biopharmaceutical / Healthcare
RECOMMENDED TRAINING
1/5
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