Anjali T
Quality Operations Professional
About
Anjali T is a pharmaceutical quality professional with extensive experience in sterile drug substance manufacturing, Quality Management Systems (QMS), and cGMP compliance. She possesses over 2.6 years of experience, specializing in Quality Assurance and Quality Operations within the pharmaceutical industry. Her expertise includes hands-on application of SAP ERP, deviation management, and CAPA documentation, ensuring robust quality frameworks. She is seeking roles that leverage her comprehensive understanding of regulatory compliance and operational excellence to drive product quality and safet
Experience
Team Member – Downstream (QMS)
Nov 2024 – Jun 2026 · 1 yr 7 mosDr. Reddy's Laboratories · Hyderabad
- Execute Quality Operations services supporting product quality compliance.
- Manage QMS documentation including change controls, deviations, and SOPs.
- Author and review CAPA documentation and root cause analyses.
Executive – Downstream
Feb 2023 – Aug 2024 · 1 yr 6 mosBiocon Biologics · Bangalore
- Ensured strict adherence to cGMP regulations and SOPs for product quality.
- Reviewed and updated Master Batch Records, ensuring regulatory alignment.
- Managed training curricula within LMS and resolved training anomalies.
Working Intern – Upstream
Jul 2022 – Jan 2023 · 6 mosBiocon Biologics · Bangalore
- Gained hands-on experience in fermentation operations and process monitoring.
- Contributed to USFDA audit readiness by ensuring documentation accuracy.
- Maintained strict cleanroom protocols upholding aseptic manufacturing practices.
Skills
Regulatory Standards
Data Management & Systems
Quality Assurance & Compliance
Pharmaceutical Manufacturing & Operations
Languages
Education & Certifications
Master of Science (M.Sc.) in Biotechnology
· 2021
Bachelor of Science (B.Sc.) in Biotechnology
· 2019
Class 12 – VHSE in Medical Laboratory Technician
· 2016
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