Senior Team Leader -Quality Assurance
Pfizer · Visakhapatnam
- Experience10–12 yrs
- SalaryNot disclosed
- Work modeonsite
- Levelexecutive
- Posted16 Sept 2026
About Pfizer
Pfizer is hiring in Visakhapatnam in pharma biotech. This role looks for around 10+ years of experience.
Skills
- Good Manufacturing Practices
- cGMP
- regulatory compliance
- sterile injectable manufacturing
- CAPA
- quality audits
- batch record review
- standard operating procedures
- people management
- quality operations
The role
A quality engineer at a pharmaceutical manufacturing company ensures sterile injectable production follows Good Manufacturing Practices, regulatory standards, and CAPA requirements, and applies statistical analysis and Laboratory Information Management System expertise to strengthen quality operations.
Full job description
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. Our dedication to quality and safety ensures that we consistently meet the highest standards, making a real difference in the lives of those we serve. As a Team Lead, you will be at the forefront of improving patients' lives while working at Pfizer.
What You Will Achieve
In this role, you will:
Lead and monitor quality over sight for operations from Solution preparation to vial/ ampoule collection in TS block to ensure compliance with respect to cGMP systems and procedures. Ensure manufacturing procedures, policies and standards confirm to pre-defined regulatory standards and corporate standards. Ensure that when quality related issues arise, they are addressed appropriately and in a timely manner as per site requirements. Manage the department in compliance with internal procedural requirements and external regulatory audits. Work with direct reports, Lead-Operations to resolve issues with compliance and comply the cGMP standards in production area. Update procedures as necessary to address continuous improvement opportunity. Ensure on line manufacturing activities, contemporaneous documentation as per the defined procedures and batch record review. Review, approve, and authorize standard operating procedures, pre R approval/certification of protocolsConduct investigation and ensure appropriate CAPA’s and effectiveness verifications. Involve site quality audits and identifying corrective and preventive actions.
Here Is What You Need (Minimum Requirements)
B.Pharma, M.Pharma or MSC10-12 years of experienceSterile injectable experience onlyPeople Management experienceAdvanced analytical skillsDemonstrated leadership skillsQuality operations technical knowledge and strong people management experienceEffective communication skills, both written and verbalThorough understanding of GMPs, applicable SOPs, production processes, and statistical/inspection practices
Bonus Points If You Have (Preferred Requirements)
Proficiency in using data analysis computer tools and conducting statistical analysisFamiliarity with Laboratory Information Management System Empower and Microsoft Office programsStrong problem-solving skills and the ability to think criticallyExcellent organizational and time management skillsStrong collaboration and team-building skillsExperience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
Work Location Assignment: On Premise
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