Quality Assurance Job for Chemistry Graduates | Pfizer Career
Are you looking for a rewarding Quality Assurance Job with one of the world’s leading pharmaceutical companies? Join Pfizer India as an Associate Manager – Quality Assurance in Chennai and become part of a global organization that transforms lives through innovation and science. In this role, you’ll ensure data integrity, compliance, and quality excellence across product development and analytical review, contributing to Pfizer’s mission to deliver breakthroughs that change patients’ lives. This is an excellent opportunity for chemistry graduates seeking to build a meaningful Pfizer career in quality assurance.
About the Company
Pfizer is a global biopharmaceutical leader committed to discovering, developing, and delivering innovative therapies that make the world a healthier place. With a culture rooted in scientific excellence, collaboration, and individual ownership, Pfizer careers empower people to drive breakthroughs that change patients’ lives. Join a team where your passion for quality, science, and compliance helps improve the future of medicine every day.
Job Details
- Job Post: Associate Manager Quality Assurance
- Job ID: 4939724
- Education: Master of Science in Chemistry
- Experience: Relevant experience in analytical data review, technology transfer, and cGMP sterile manufacturing areas.
- Work Location: On-Premise – Chennai
Role Summary
As an Associate Manager – Quality Assurance, you will be responsible for reviewing documents related to product development, analytical data (including electronic data, chromatographic data, and audit trails), as well as instrument and equipment qualification. You will ensure data integrity compliance and adherence to SOPs during the review of both hard copy and electronic records, making this an ideal Quality Assurance job for chemistry graduates looking to advance their Pfizer career.
Key responsibilities include
- Conduct periodic system audit trail reviews and ensure compliance with 21 CFR Part 11 requirements.
- Collaborate with global BL and OQ colleagues to achieve organizational objectives.
- Maintain in-depth understanding of ICH quality guidelines and regulatory guidance on microbiology method development for sterility, BET, CCIT, and related requirements.
- Demonstrate expertise in sterility requirements and filter validation as per PDA technical reports.
- Possess familiarity with sterile ANDA product development and combination products.
- Exhibit strong proficiency in MS Office applications, including Excel, Word, and PowerPoint.
Role Responsibilities & Skill Sets:
- Awareness of Data Integrity (DI) and ALCOA principles.
- Understanding of cGMP requirements, including 21 CFR Part 210 and 211, ICH guidelines, and sterile product standards.
- Maintain compliance in laboratories and during document review.
- Perform statistical evaluation and analysis of analytical data during method development and validation review.
- Demonstrate effective communication, discipline, and self-motivation.
- Support QA initiatives to improve consistency, efficiency, and compliance.
- Manage time effectively to meet project deadlines.
- Contribute to continuous improvement and procedural development within quality and business lines.
- Support inspection readiness, internal audits, and regulatory inspections as required.
