Hridya Uday

Armed with a Master's degree in Pharmaceutical Sciences, I bring a comprehensive understanding of drug development, regulatory compliance, and industry best practices. Specialized in drug formulation, pharmacovigilance, and regulatory affairs with a keen eye for detail in executing research and development initiatives. A proactive thinker committed to staying abreast of industry trends and emerging technologies to contribute to cutting-edge pharmaceutical solutions. Experienced in collaborating with diverse teams and adapting to dynamic international environments, fostering cross-functional partnerships. My passion lies in leveraging pharmaceutical science to make a positive impact on global health. I am excited about contributing my skills and knowledge to a forward-thinking organization that values innovation, collaboration, and a commitment to excellence.

I am a results-driven MSc in Pharmaceutical Business & Technology graduate with a Bachelor of Pharmacy and proven experience across pharmaceutical manufacturing, clinical research, laboratory operations, and healthcare support services.

Currently working as a Production Operator at Jabil, where I ensure GMP and ISO 13485 compliance, operate precision equipment, support CAPA investigations, and promote lean initiatives.

Previously employed as a Clinical Research Associate at IQVIA, specializing in pharmacovigilance, regulatory compliance, and clinical data management across therapeutic areas.

Earlier experience includes roles as a Laboratory Assistant and Hospital Pharmacist Trainee, where I gained hands-on expertise in HPLC analysis, equipment calibration, LIMS, TrackWise, and SAP, along with medication dispensing and patient support.

Strong foundation in quality systems, audit readiness, and regulatory adherence, with skills in analytical techniques, documentation, and cross-functional teamwork.

Recognized for attention to detail, problem-solving, and adaptability, I bring a well-rounded background that combines technical expertise, clinical insight, and regulatory knowledge to support operational excellence in healthcare and life sciences.

I hold an MSc in Pharmaceutical Business & Technology from Griffith College Dublin (Innopharma Education), where I gained expertise in pharmaceutical manufacturing, regulatory compliance, and process optimization. My thesis focused on segregation in the manufacturing of solid dosage forms, reflecting my strong analytical and research skills.

I also hold a Bachelor of Pharmacy from JSS University, India, which provided me with a solid foundation in pharmacology, pharmaceutical sciences, and clinical practice, further strengthening my understanding of medicines, patient safety, and healthcare delivery.