PHARMAFull-time
Associate
VIZAG (IN)ONSITEPOSTED: 8/11/2026
PHARMAFull-time
HIRING ORGANIZATIONPFIZERBiopharmaceutical / Healthcare
ROLE DEFINITION & RESPONSIBILITIES
Evaluate, review, and approve validation master plans, protocols, and reports in compliance with cGMP regulations.
Troubleshoot validation issues for equipment and processes, performing statistical analysis on test results.
Draft, review, and finalize technical reports and validation documentation for laboratory and manufacturing equipment.
Determine process capability for new equipment and assist in deviation investigations to define CAPAs.
Collaborate with Quality Operations training teams to support cGMP standards and site training programs.
REQUIRED VERIFIED SKILLS
cGMP
Validation Protocols
Technical Writing
Data Analysis
Equipment Qualification
MS Excel
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
READY TO SUBMIT?
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