Use Your Power for Purpose

Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:
Prepare and review essential documentation, including GMP, GLP, and GCP manuals.
Responsible and Managing of Document Management Life Cycle and Record Management
Issuance, Retrieval, Archival and Control of GMP Documents/Records and DSMs (GMP documents) through Manual and Electronic systems.
Secure bin management
Knowledge on PDOCs, p-log and SDS Applications
Ensure compliance with Enterprise Records Retention Schedule (ERRS) maintained by the enterprise records and Information Management (eRIM) group.
Location mapping & tracking of documents/ records archived in Active Record Centers.
Competency in MS office,



Adobe Acrobat and documentation data base systems
Execute tasks supporting Quality Systems functions and oversee Documentation Control and administrative functions of the DMS repository.

Here Is What You Need (Minimum Requirements):
Bachelor's Degree (Chemistry/Pharmacy) with 4+ Years of Experience or Master's Degree (Chemistry/Pharmacy) with 3+ Years of Experience
Proficiency in Document Management and Control
Experience with Computer Software Validation Concepts
Familiarity with regulatory requirements and compliance standards
Effective communication skills

Bonus Points If You Have(Preferred Requirements):
Project Planning experience
Lean or Six Sigma experience
Knowledge of Valuable Manufacturing Practices (GMP) and Good Laboratory Practices (GLP)
Solid problem-solving skills
Excellent time management and organizational skills
Adaptability in a dynamic work workplace
Experienc

📌 Associate Quality Systems Visakhapatnam
🏢 Pfizer
📍 Visakhapatnam