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    Associate Manager Quality Assurance Job At Pfizer Chennai | Apply Now

    Associate Manager Quality Assurance Job At Pfizer

    Discover an excellent opportunity at Pfizer as an Associate Manager in Quality Assurance based in Chennai. This QA Job role focuses on analytical data review, sterile product development oversight, compliance with global quality standards, and ensuring data integrity across pharmaceutical processes. Graduates seeking for M Pharma jobs and who want to start their career with Pfizer Careers can apply now.

    Job Details

    • Job Title: Associate Manager Quality Assurance
    • Location: Chennai, India

    About the Company

    Pfizer is a global leader in pharmaceuticals, committed to delivering innovative treatments and maintaining the highest levels of quality and compliance. With a strong legacy in sterile manufacturing, Pfizer ensures global standards of safety, efficacy, and regulatory excellence across its operations.

    Educational Requirements for QA Job Role

    Key Responsibilities 

    • Review documents related to product development and analytical data
    • Ensure accurate evaluation of electronic data, chromatographic data, and audit trails
    • Maintain strict data integrity compliance and adherence to SOPs
    • Conduct periodic system audit trail reviews per 21 CFR Part 11
    • Collaborate with global BL and OQ teams
    • Understand ICH guidelines and regulatory expectations for microbiology methods
    • Supporting sterility testing, BET, CCIT, filter validation, and sterile ANDA development is essential for the QA Job
    • Demonstrate strong MS Office skills for documentation and presentations
    • Maintain compliance during lab operations and document review
    • Perform statistical evaluation of analytical data during development and validation
    • Communicate effectively and work with discipline and self-motivation
    • Contribute to QA initiatives, continuous improvement, and new goals
    • Support inspection readiness, internal audits, and regulatory inspections
    • Suggest improvements and participate in procedure development
    • Manage timelines and plan work activities for assigned projects

    Skills Required for QA Job Role

    • Knowledge of Data Integrity and ALCOA principles
    • Basic understanding of cGMP, 21 CFR 210/211, and ICH guidelines
    • Awareness of sterile product requirements
    • Ability to review analytical data with statistical analysis
    • Strong communication and organizational skills
    • Expertise in MS Excel, Word, and PowerPoint
    • Ability to support Technology Transfer activities
    • Self-motivation, discipline, and the ability to work independently
    • Continuous improvement mindset

    CLICK HERE FOR OFFICIAL NOTIFICATION

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