Krishnapriya K Email & Phone Number

Hyderabad, Telangana, India

Chennai, Tamil Nadu

𝑲𝒆𝒚 𝑹𝒆𝒔𝒑𝒐𝒏𝒔𝒊𝒃𝒊𝒍𝒊𝒕𝒊𝒆𝒔 –❖ 𝐀𝐧𝐚𝐥𝐲𝐭𝐢𝐜𝐚𝐥 𝐌𝐞𝐭𝐡𝐨𝐝𝐨𝐥𝐨𝐠𝐲 𝐃𝐞𝐯𝐞𝐥𝐨𝐩𝐦𝐞𝐧𝐭: Contributed significantly to regulatory starting materials and drug substance research and development projects by spearheading the creation of cutting-edge analytical methodologies. Mastered advanced analytical techniques, including liquid chromatography, ensuring a comprehensive skill set in analytical science. ❖ 𝐑𝐞𝐚𝐜𝐭𝐢𝐨𝐧 𝐌𝐨𝐧𝐢𝐭𝐨𝐫𝐢𝐧𝐠 𝐚𝐧𝐝 𝐑𝐚𝐰 𝐌𝐚𝐭𝐞𝐫𝐢𝐚𝐥 𝐀𝐧𝐚𝐥𝐲𝐬𝐢𝐬: Vigilantly monitored reactions and conducted detailed analysis of raw materials , intermediates and API using HPLC, ensuring the quality and consistency of essential components.❖ 𝐈𝐧𝐧𝐨𝐯𝐚𝐭𝐢𝐯𝐞 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧𝐬 𝐚𝐧𝐝 𝐄𝐟𝐟𝐢𝐜𝐢𝐞𝐧𝐜𝐲: Championed the integration of new technologies, process enhancements, and informatics initiatives to enhance operational efficiency and compliance. Led the successful implementation of the 5S methodology and maintenance practices for a streamlined and organized work environment. ❖ 𝐐𝐮𝐚𝐥𝐢𝐭𝐲 𝐚𝐧𝐝 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐂𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐜𝐞: Ensured strict adherence to quality and regulatory requirements, including ALCOA++ principles, ICH guidelines, cGMP, 21CFR, and Pfizer SOPs. Navigated and handled rigorous Regulatory Quality Assurance (RQA) audit, demonstrating a commitment to maintaining high standards of quality, compliance, and best practices in all aspects of our operations. ❖ 𝐂𝐨𝐥𝐥𝐚𝐛𝐨𝐫𝐚𝐭𝐢𝐯𝐞 𝐏𝐫𝐨𝐛𝐥𝐞𝐦 𝐒𝐨𝐥𝐯𝐢𝐧𝐠: Collaborated seamlessly with team members to select the most suitable analytical tools, often incorporating computational predictive tools, modeling software, and data visualization tools to enhance project outcomes.

Chennai, Tamil Nadu, India

𝑲𝒆𝒚 𝑹𝒆𝒔𝒑𝒐𝒏𝒔𝒊𝒃𝒊𝒍𝒊𝒕𝒊𝒆𝒔 – ❖ 𝐄𝐥𝐞𝐜𝐭𝐫𝐨𝐧𝐢𝐜 𝐑𝐞𝐜𝐨𝐫𝐝 𝐊𝐞𝐞𝐩𝐢𝐧𝐠: Employed Bio via Electronic Laboratory Notebook (ELN) to systematically record all experiments, maintaining a comprehensive and organized database of research activities. ❖ 𝐄𝐪𝐮𝐢𝐩𝐦𝐞𝐧𝐭 𝐌𝐚𝐧𝐚𝐠𝐞𝐦𝐞𝐧𝐭 𝐚𝐧𝐝 𝐒𝐚𝐟𝐞𝐭𝐲: Demonstrated a strong commitment to maintaining laboratory instruments and systems, ensuring their reliability and longevity. Consistently upheld safe working practices and actively contributed to continuous improvements in lab safety. ❖ 𝐂𝐨𝐨𝐫𝐝𝐢𝐧𝐚𝐭𝐢𝐨𝐧 𝐨𝐟 𝐒𝐭𝐚𝐛𝐢𝐥𝐢𝐭𝐲 𝐒𝐭𝐮𝐝𝐢𝐞𝐬: Managed and coordinated stability studies for multiple Active Pharmaceutical Ingredients (APIs), contributing to the generation of crucial initial data.❖ 𝐈𝐧-𝐏𝐫𝐨𝐜𝐞𝐬𝐬 𝐒𝐚𝐦𝐩𝐥𝐞 𝐓𝐞𝐬𝐭𝐢𝐧𝐠: Conducted in-process sample testing using HPLC and UPLC, including the assessment of purity and assay, ensuring the integrity of the production process. ❖ 𝐃𝐨𝐜𝐮𝐦𝐞𝐧𝐭𝐚𝐭𝐢𝐨𝐧 𝐚𝐧𝐝 𝐂𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐜𝐞: Meticulously maintained comprehensive written records of all experimental work in full compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards, aligning with departmental philosophies.

Master Of Science - Ms, Chemistry

Bachelor Of Science - Bs, Chemistry