Associate - Quality Systems in Visakhapatnam, भारत

Pfizer seeks an Associate for Quality Systems in Vizag to manage GMP documentation, records, and compliance processes. The role ensures pharmaceutical products meet quality standards through document lifecycle management and adherence to regulatory requirements.

Responsibilities

• Manage GMP documents and records including issuance, retrieval, archival, and disposition
• Administer document lifecycle processes from creation through obsolescence and archival
• Oversee logbook management, secure bin management, and document storage administration
• Execute change control and quality systems processes with impact assessment
• Review audit trails, verify metadata, and ensure compliance with enterprise records retention schedules

Requirements

• Bachelor's in Pharmacy, Master's in Pharmacy, or MSc with 1-4 years pharmaceutical industry experience
• Proficiency in document management and digital applications
• Strong written and verbal communication skills with cross-functional collaboration ability
• Willingness to work shift-based operations as needed
• Knowledge of GMP document and record management practices
• Familiarity with document lifecycle management and records retention schedules
• Experience with AI tools such as ChatGPT or Microsoft Copilot (preferred)