Shivani S

WORK HISTORY

EDUCATION

ABOUT SHIVANI S

I am a Quality Control and analytical laboratory professional with ~3 years of experience across analytical testing, biologics QC, deeply passionate about building smoother, higher-performing quality control systems.Currently, a QC scientist at GSK\'s Augmentin manufacturing site where I combine technical expertise in penicillin testing with a strong leadership role in coordinating lab operations and managing instrument lifecycles. Also leading a proactive, QC lab safety transformation project to optimize laboratory working conditions and compliance.My background further spans GMP-regulated pharmaceutical testing, where I supported the release of large-molecule biologics (mAbs and CSFs) through HPLC, SDS-PAGE, IEF, ELISA, and stability testing, as well as OOS/OOT investigations, audit readiness, and instrument calibration at Dr. Reddy’s Laboratories.In addition to my analytical responsibilities, I was appointed Safety Single Point of Contact for the Quality Analytics team, where I led safety communications, training, and chemical exposure monitoring, and was recognised as one of the team’s leading QC analysts, entrusted with complex analyses, investigations, and critical batch release timelines.More recently, I found my passion for Bioinformatics when I became a part of the laborious and energy exhaustive R&D involved in traditional Drug Discovery and Development process. My MSc at the University of Bristol strengthened my analytical thinking through proteomics, RNA-seq, and bioinformatics workflows, translating complex datasets into clear insights. Across both industry and academia, I bring a strong commitment to data integrity, safety, and collaboration, and I am motivated by contributing reliable, meaningful science in regulated research environments.With a strong foundation in GMP testing, validation, and laboratory operations, I am looking to transition into a QC Lead or Senior Quality Control role. I am passionate about mentoring, spearheading root-cause investigations, and introducing continuous improvement methodologies (like Lean or Six Sigma) to elevate pharmaceutical manufacturing standards.