QA Job at Pfizer | MSc Chemistry Graduates Apply Now
Are you looking for a rewarding Quality Assurance Job in the pharmaceutical industry? Pfizer is hiring an Associate Manager Quality Assurance in Chennai, offering the perfect opportunity for professionals exploring QA Jobs or aiming to advance within Pfizer careers. This role provides exposure to analytical data review, data integrity, regulatory compliance, and sterile product development, making it an excellent fit for candidates seeking long-term growth in a top global pharmaceutical company.
About Pfizer
Pfizer is one of the world’s leading biopharmaceutical companies, dedicated to discovering, developing, and delivering innovative healthcare solutions. As a global organization committed to scientific excellence, Pfizer provides outstanding opportunities for professionals seeking growth through Pfizer careers, especially in areas such as data integrity, quality compliance, and sterile product development. Whether you aspire to progress in QA Jobs or build a long-term career in quality systems, Pfizer offers an environment driven by innovation, collaboration, and continuous improvement.
Job Details
- Position: Associate Manager Quality Assurance
- Locations: India – Chennai
- Job Requisition ID: 4939724
- Qualification: Master of Science in Chemistry
- Experience: Relevant work experience in an analytical data review, technology transfer, and cGMP pharmaceutical sterile manufacturing area
Job description
Responsible for reviewing product development documents, analytical data, audit trails, and qualification records while ensuring data integrity and SOP compliance. The role includes periodic audit trail reviews, adherence to 21 CFR Part 11, and collaboration with global BL and OQ teams. It requires strong knowledge of ICH guidelines, sterility methods, BET, CCIT, PDA reports, filter validation, and sterile ANDA development. Proficiency in MS Office is essential. This Quality Assurance Job is ideal for professionals pursuing QA Jobs and those seeking long-term growth through Pfizer careers in quality systems, regulatory compliance, and sterile product development.
Responsibilities
- Awareness of DI and ALOCA principles
- Basic understanding of cGMP requirements, including 21 CFR parts 210 and 211, ICH guidelines, and sterile product requirements
- Maintain compliance in laboratories and during document review
- Ability to perform statistical evaluation and analysis of analytical data during method development and validation review
- Effective communication skills.
- Adherence to discipline and self-motivation.
- Participate in implementing new initiatives and goals within the QA function and with business line partners to support consistency, efficiency, and compliance.
- Manage time to meet agreed-upon targets and plan project work activities for assigned teams.
- Suggest improvements and participate in continuous improvement activities.
- Contribute to the development and compliance of quality and business line partner procedures.
- Provide support for inspection readiness efforts, internal audits, and regulatory inspections as required.
