Swati Gupta

About Swati Gupta

M.Sc. Analytical Chemistry graduate with 3+ years’ experience in wet lab analysis, documentation, and compliance support in the biotech sector. Skilled in enzyme analysis, analytical testing (HPLC, UV, Galleryplus), method validation, SOP-based operations, and technical reporting.Currently upskilling in Good Documentation Practices (GDP) and Regulatory Affairs to expand my expertise into QA Executive, Project Executive, Regulatory Affairs, Clinical Research, and Medical/Scientific Writing roles.Key Competencies: GMP, GLP, Documentation, Data Integrity, CAPA (basic), Audit Preparation, Regulatory Submissions, QA/QC, R&D Support, Scientific Writing.Recognized for accuracy, attention to detail, and clear documentation, I aim to contribute to regulated environments by ensuring compliance, maintaining quality standards, and supporting operational excellence.Open to opportunities in Mumbai and Pune across pharma, CRO, chemicals, or healthcare domains. Let’s connect if you are looking for a quality-focused, adaptable life sciences professional ready to contribute from day one.

Experience

1. Lab Analyst

   Zytex

   Oct 2021 — Present

   As a Lab Analyst with a post-graduate background in Analytical Chemistry, I specialize in enzyme analysis, supporting product quality through accurate and timely technical testing. My role involves analytical testing, documentation, and collaboration with internal teams to ensure consistency and reliability in lab outputs.Key Responsibilities:Perform enzyme activity analysis on raw materials and finished products using internal protocols and wet chemistry techniques.Prepare reagent solutions, calibrate instruments, and maintain logs for traceability and repeatability.Record and organize test data with attention to accuracy and clarity to support internal quality systems.Collaborate with technical and production teams for timely sample analysis, troubleshooting, and reporting.Maintain a clean, safe lab environment and adhere to established internal procedures and safety norms.Key Achievements:Reduced reporting turnaround time by coordinating with cross-functional teams, improving lab-to-production communication efficiency.Trained junior staff on enzyme testing protocols, documentation procedures, and safety measures.Additional Development:Self-learning industry standards such as GMP, GLP, and Regulatory Documentation to prepare for roles in QA, Regulatory Affairs, and Clinical Research.Enhancing skills in scientific writing, documentation, and technical communication to support cross-functional roles.

Education

• RAMNIRANJAN JHUNJHUNWALA COLLEGE

  Bachelor's degree

  2015 — 2018

• SNDT Women's University - P. G. Department of Analytical Chemistry

  Master's degree

  2018 — 2020