PHARMAFull-time
Manager - Quality Compliance
VIZAG (IN)ONSITEPOSTED: 8/12/2026
PHARMAFull-time
HIRING ORGANIZATIONPFIZERBiopharmaceutical / Healthcare
ROLE DEFINITION & RESPONSIBILITIES
Lead site Quality Compliance and Data Integrity governance programs across manufacturing, QC labs, warehouses, and engineering.
Perform routine GxP data integrity assessments and ALCOA+ gap analyses, driving sustainable CAPA implementations.
Oversee root cause investigations, product market complaints, CAPA effectiveness checks, and Annual Product Reviews.
Drive regulatory inspection readiness for international audits (US FDA, MHRA, EMA, WHO, TGA) and host compliance walkthroughs.
Design and deliver site-wide training programs focusing on data integrity, GxP regulations, and quality compliance.
Present compliance trends, risk evaluations, and data integrity metrics to leadership during Quality Management Reviews.
REQUIRED VERIFIED SKILLS
Quality Assurance
Quality Compliance
Data Integrity
ALCOA+
Root Cause Analysis
CAPA
Investigation Management
US FDA Inspections
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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