Sandra Saji
Quality Assurance professional with 2.5 years of GMP pharmaceutical experience, skilled in Documentation QA and Quality Management Systems in both OSD and softgel manufacturing environments.
AI analysis: Personality & work environments
The content in this CV is automatically created by SuperRen after an AI conversation, where Sandra Saji shared his experiences, skills and personal strengths.
Work environments
Experienced in quality assurance roles primarily within the pharmaceutical sector, working in various manufacturing settings with a strong focus on compliance and audit readiness.
As a person
Demonstrates a strong commitment to detail and procedures, indicating reliability and a professional work ethic. Shows flexibility in work arrangements and a readiness to adapt to team or independent settings.
Previous experience
Softgel Healthcare Pvt. Ltd.
Team Member – QA
Dec 2025 – Jul 2026
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Managed QMS activities including CAPA, change control, Market compliant and deviation management. Supported internal and external audits with audit-ready documentation.
Highlights hands-on experience in quality management systems and a proactive approach in audit preparations.
Sunglow Lifescience Pvt. Ltd.
Officer – QA
Jul 2023 – Aug 2025
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Handled SAP QA activities including item code, BOM, manufacturing orders, and batch release. Prepared and compiled Process Validation and Hold Time Study reports.
Indicates strong familiarity with SAP systems and emphasizes capacity for managing comprehensive quality processes.
Education
Central University of Pondicherry
M.Sc. Biochemistry and Molecular BiologyGraduated with a CGPA of 8.6.