Arintika H

Arintika H. is a dedicated QC Stability Analyst at Abbott, leveraging her strong background in chemistry and extensive expertise in pharmaceutical quality control to ensure the highest standards of product stability and safety. With a Bachelor of Science degree in Chemistry and certification from BNSP in chemical analysis—ranging from conventional to instrumental methods—she brings a comprehensive understanding of analytical techniques and laboratory safety protocols, including Laboratory EHS compliance. Her current role involves performing detailed chemical analyses on scheduled stability samples, which is critical for verifying product shelf-life and ensuring compliance with regulatory standards.

In her position, Arintika is responsible for executing stability protocols, preparing stability reports, and managing climatic chambers as the Person in Charge (PIC). She oversees the charging of new samples and the retrieval of pull samples, meticulously monitoring environmental conditions to maintain sample integrity. Her proficiency in analyzing stability trend data using Minitab allows her to identify potential deviations early, supporting data-driven decision-making for product release and shelf-life extension. Her expertise in trend data stability analysis, combined with her leadership skills, enables her to coordinate cross-functional teams effectively and uphold rigorous quality standards.

Arintika’s skill set encompasses a broad spectrum of analytical techniques, including volumetric analysis, microbiological testing, proximate analysis, atomic absorption spectroscopy, and FTIR. Her comprehensive knowledge of laboratory management, combined with her analytical acumen and leadership qualities, makes her a valuable asset in maintaining Abbott’s commitment to pharmaceutical excellence. Her proactive approach and industry-specific expertise ensure that stability testing processes are conducted efficiently, accurately, and in compliance with Good Laboratory Practices (GLP) and regulatory requirements.