Sowmiya Nssr

Quality and process-focused professional with 5 years of experience in QA/QC within the biotechnology and enzyme industry. Experienced in quality monitoring, internal audits, QMS, SOP creation and review, regulatory documentation, deviation tracking, data interpretation, process coordination and team training. Demonstrated process-improvement impact by reducing deviation closure time by 20% through improved documentation tracking.

Strong attention to detail, documentation accuracy, cross-functional collaboration and operational quality, with a strong interest in Quality Analyst and Process Improvement roles.

Senior QA/QC - Fleurveda Private Limited

(2024-09)

• Analyzed raw materials, labeling and packaging materials to ensure compliance with FDA, ISO and BIS requirements.
• Maintained QA documentation and calibration records for biochemical and microbiology laboratories.
• Supported internal audits and ensured adherence to QMS protocols and GMP requirements.
• Performed scientific data analysis and maintained accuracy and completeness of quality documentation.
• Conducted rigorous quality monitoring, data collection, and internal audits for operational batch records, ensuring full compliance with regulatory standards and zero critical observations.

QA/QC Executive - Senthil Papain Private Limited

(2021-03 - 2023-12)

• Performed analysis of raw materials, in-process samples and finished products under applicable quality and ISO standards.
• Prepared and reviewed SOPs, HACCP plans and Certificates of Analysis (COA), supporting consistent process execution.
• Maintained documentation in line with USP, IP, WHO-GMP, ISO 9001, ISO 22000 and FSSAI requirements.
• Trained team members in quality testing, sample handling and documentation procedures.
• Managed audit records, deviation logs and customer complaint documentation, supporting timely issue resolution.
• Coordinated quality testing, purity assessment and process activities across operational teams.
• Maintained and calibrated laboratory instruments including spectrophotometer, HPLC, muffle furnace, stability chamber and laminar air flow.
• Reduced deviation closure time by 20% through improved documentation tracking.
• Led internal QA audits for enzyme batch records with zero critical observations.

B.Sc. - Biotechnology - AJK College of Arts and Science

Diploma - Medical Laboratory Technology (DMLT) - AJK College of Arts and Science

Higher Secondary

Secondary