Liya Siby

• Integral member of the drug product development department, specializing in stability team.
• Proficient in High Performance Liquid Chromatography (HPLC) techniques, UV Visible spectroscopy, SDS PAGE for analytical testing and quality assurance in drug product development.
• Execute stability studies, managing charging and pulling out of samples at specified time points.
• Perform appearance and particle tests to ensure product quality and compliance with specifications.
• Adhere to and enforce Good Laboratory Practices (GLP), ensuring integrity and reliability of analytical results.
• Apply Good Documentation Practices (GDP) for accurate and comprehensive record-keeping.
• Implement Good Manufacturing Practices (GMP) to maintain high-quality standards throughout drug product development.
• Collaborate closely with cross-functional teams to contribute to the success of drug product development initiatives.

• Provided clerical support, addressing routine, and special requirements.
• Engaged in downstream purification of monoclonal antibodies, gaining hands-on experience in purification techniques.
• Contributed to method development under the mentorship of experienced professionals.
• Assisted in data analysis, documentation, and presentation of findings to support ongoing research and development efforts.
• Gained valuable insights into the application of industry best practices and quality standards within a research and development setting.

Engaged in a virtual internship focused on insilico biologic's, gaining practical experience in software applications related to protein sequencing

Proficient in utilizing tools such as NCBI, BLAST, and PubMed for comprehensive data analysis and bioinformatics research.