Associate - Quality Systems
Associate - Quality Systems
Pfizer- Posted 11 hours ago
- Be among the first 10 applicants
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:
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
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.
- 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
- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance
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
More Info
Key Skills
change control impact assessment
document management digital applications
secure bin management
electronic document management systems
CICR
PDOCs
GMP Document and Record Management
document storage administration
Enterprise Records Retention Schedule (ERRS)
p-Log
logbook management
Quality Systems processes
