Associate - Quality Systems
Pfizer · Visakhapatnam
- Experience1–4 yrs
- SalaryNot disclosed
- RoleLab & Pharma Scientist
- Work modeonsite
- Posted13 Oct 2026
About Pfizer
Pfizer is hiring in Visakhapatnam in pharma biotech. This role looks for around 1+ years of experience.
Skills
- GMP
- Document Lifecycle Management
- Enterprise Records Retention Schedule (ERRS)
- change control
- impact assessment
- Document management digital applications
- Microsoft Copilot
- ChatGPT
The role
Quality systems associate at a pharmaceutical company. Applies pharmaceutical quality systems and GMP document and record management to control document lifecycles, records retention, change control, and compliance. Uses Document management digital applications and Microsoft Copilot.
Full job description
Use Your Power for Purpose
Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.
What You Will Achieve
In this role, you will:
.
Knowledge of GMP Document and Record Management, including document issuance, retrieval, archival, retention, and disposition.
Knowledge of PDOCs, SDS, p-Log, Therefore, CICR, and electronic document management systems.
Knowledge of official print management, audit trail review, metadata verification, document scanning, and record tracking.
Understanding of Document Lifecycle Management, including document creation, review, approval, issuance, archival, retrieval, retention, and obsolescence.
Familiarity with Enterprise Records Retention Schedule (ERRS) requirements and records compliance practices.
Knowledge of logbook management, secure bin management, and document storage administration.
Understanding of change control, impact assessment, and Quality Systems processes.
Experience using AI-powered tools, such as Microsoft Copilot and ChatGPT, to enhance productivity, streamline workflows, and improve operational efficiency.
Here Is What You Need (Minimum Requirements)
B.Pharma, M.Pharma or MSC with 1 to 4 years of relevant experience in the pharmaceutical industry.
Willingness to work in shifts-based operations as required by business needs.
Strong written and verbal communication skills with the ability to collaborate effectively across functions.
Document management digital applications experience
Bonus Points If You Have (Preferred Requirements)
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.