PHARMAFull-time
Associate
VIZAG (IN)ONSITEPOSTED: 8/11/2026
PHARMAFull-time
HIRING ORGANIZATIONPFIZERBiopharmaceutical / Healthcare
ROLE DEFINITION & RESPONSIBILITIES
Review and approve validation master plans, technical reports, and protocols.
Troubleshoot equipment and performance process issues through statistical analysis of test results.
Execute protocols to establish process capabilities for new equipment and update operating procedures.
Assist in developing validation protocols, handling regulatory inquiries, and managing deviation root-cause analysis.
Collaborate with Quality Operations teams to ensure adherence to cGMP, site training initiatives, and safety regulations.
REQUIRED VERIFIED SKILLS
cGMP
Validation Master Plans
Equipment Qualification
Statistical Analysis
Process Validation
Quality Operations
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
1/2
READY TO SUBMIT?
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