PHARMAFull-time
Associate
VIZAG (IN)ONSITEPOSTED: 8/12/2026
PHARMAFull-time
HIRING ORGANIZATIONPFIZERBiopharmaceutical / Healthcare
ROLE DEFINITION & RESPONSIBILITIES
Evaluate, review, and approve validation master plans, protocols, and technical execution reports.
Perform statistical analysis on testing results and troubleshoot validation/performance anomalies across equipment and processes.
Execute approved equipment qualification protocols, establish process capabilities, and integrate parameters into batch records.
Assist in deviation investigations to determine root causes and implement Corrective and Preventive Actions (CAPA).
Support site cGMP training initiatives and maintain full adherence to FDA regulations, SOPs, and quality safety standards.
REQUIRED VERIFIED SKILLS
Validation Protocols
Equipment Qualification
cGMP
FDA Regulations
CAPA
Deviation Investigation
Statistical Analysis
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
1/4
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