Associate Manager Quality Assurance – Pfizer Careers Chennai | Apply Now
Build your future with Pfizer careers through this exciting opening for an Associate Manager Quality Assurance role in Chennai. This opportunity is ideal for professionals seeking Quality Assurance jobs in the pharmaceutical industry, especially those experienced in analytical data review, sterile product development, regulatory compliance, and cGMP operations. Explore the full job description, responsibilities, qualifications, and company details below.
Job Details:
- Job Title: Associate Manager Quality Assurance
- Locations: India – Chennai
- Job Requisition ID: 4939724
About The Company:
Pfizer is a global leader in the pharmaceutical industry dedicated to bringing innovative therapies to patients that significantly improve their lives. With a strong commitment to scientific research and development, Pfizer constantly seeks talented individuals to join the team and contribute to our mission of advancing health and well-being around the world.
Job Description | Quality Assurance Jobs at Pfizer:
The Associate Manager Quality Assurance position involves review of product development documents, analytical data, equipment qualification, and compliance with data integrity principles. This role supports sterile product development, regulatory guideline adherence, and global quality operations collaboration within Pfizer.
Key Responsibilities at Pfizer Careers :
- Review documents related to product development, analytical data (electronic & chromatographic), and audit trails.
- Ensure data integrity and adherence to SOPs for both electronic and hard copy records.
- Conduct periodic system audit trail reviews ensuring 21 CFR Part 11 compliance.
- Liaise with global BL and OQ colleagues.
- Maintain understanding of ICH quality guidelines, microbiology method development (sterility, BET, CCIT).
- Understand sterility requirements and filter validation per PDA technical reports.
- Demonstrate knowledge of sterile ANDA product development and combination products.
- Proficient in MS Office – Excel, Word, PowerPoint.
- Awareness of DI and ALOCA principles.
- Basic understanding of cGMP, 21 CFR 210/211, and sterile product regulations.
- Perform statistical evaluation and analysis of analytical data.
- Maintain laboratory and document review compliance.
- Strong communication, discipline, and self-motivation.
- Support QA initiatives for efficiency and compliance.
- Plan activities to meet targets and project timelines.
- Suggest improvements and participate in continuous improvement.
- Support inspection readiness, internal audits, and regulatory inspections.
Qualifications Required For Pfizer Careers
Education:
- Master of pharmacy
Relevant Experience:
- Relevant work experience in an analytical data review and Technology transfer and cGMP pharmaceutical sterile manufacturing area
