Pfizer Quality Assurance Associate: B.Pharm/M.pharm, MSc(Microbiology/Chemistry)

• Pfizer Quality Assurance Associate: Ensuring Compliance and Excellence
• About Pfizer
• Role: Quality Assurance Associate
• Qualifications and Requirements
• APPLY ONLINE 

Pfizer Quality Assurance Associate: Ensuring Compliance and Excellence

Are you an individual with a passion for maintaining high-quality standards and ensuring regulatory compliance in the pharmaceutical industry? Pfizer, a global leader in the field, is offering an exciting opportunity to work as an Associate in Quality Assurance. If you have the qualifications and dedication required for this role, read on to discover how you can be a part of Pfizer’s commitment to excellence.

About Pfizer

Pfizer is a renowned pharmaceutical company with a history of innovation and commitment to improving global health. With a focus on developing, manufacturing, and delivering innovative medicines and vaccines, Pfizer has become a trusted name in the healthcare industry.

Role: Quality Assurance Associate

As a Quality Assurance Associate at Pfizer’s location in Vizag, India, you will play a crucial role in ensuring the highest standards of quality and compliance in various manufacturing operations. Your responsibilities will include:

1. Ensuring cGMP Compliance: You will be responsible for maintaining the operating state of current Good Manufacturing Practice (cGMP) compliance in solution/emulsion preparation, vial/ampoule washing, depyrogenation, filling, and capping operations.
2. Regulatory Compliance: You will maintain regulatory compliance in accordance with cGMP practices, ensuring that all manufacturing policies and procedures adhere to Pfizer’s standards.
3. Review and Assessment: You will review electronic batch records (eBR) and assess the impact of any deviations or exceptions. Your technical support and inputs will be crucial in this process.
4. Batch Reports and Equipment Audit Trails: You will review batch reports and equipment audit trails, contributing to the accuracy and quality of manufacturing records.
5. Process Monitoring: You will monitor manufacturing practices, ensuring that they align with approved procedures and standards. Daily walk-throughs and observations will be part of your routine.
6. Troubleshooting and Efficiency Improvement: You will possess troubleshooting abilities in the manufacturing area, actively identifying gaps in processes and procedures. Your input will contribute to process simplification, reduced downtime, and increased efficiency.

Qualifications and Requirements

To be eligible for this role, you should have the following qualifications:

• B.Pharm/M.Pharm or MSc in Microbiology/Chemistry
• 1-5 years of relevant experience

APPLY ONLINE