Vishakha Oza
About Vishakha Oza
Vishakha Oza is a Pharmacovigilance Product Lead at Procter & Gamble with extensive experience in clinical safety, regulatory affairs, and strategic planning within the pharmaceutical industry.
Current Role at Procter & Gamble
Vishakha Oza is currently employed at Procter & Gamble in the role of Pharmacovigilance Product Lead since 2019. She operates out of the Darmstadt Area in Germany. In her capacity, she ensures the safety and efficacy of pharmaceutical products by monitoring and managing adverse drug reactions and other pharmaceutical safety concerns.
Past Experience at Grünenthal Group
From 2017 to 2019, Vishakha Oza worked at the Grünenthal Group in Aachen, North Rhine-Westphalia, Germany, as the Global Safety Lead Scientist Pharma. She was responsible for overseeing global safety protocols and ensuring the pharmaceutical products met stringent safety standards. Her role involved overseeing clinical safety measures and regulatory compliance.
Educational Background
Vishakha Oza holds a Bachelor’s and a Master’s degree in Pharmaceutical Sciences from Nagpur University. She furthered her education by obtaining a Diploma in Business Management from Bharatiya Vidya Bhavan between 2007 to 2008. Additionally, she has an MBA in International Healthcare Management from the Frankfurt School of Finance & Management. Her diverse educational background provides a strong foundation for her roles in pharmacovigilance and regulatory affairs.
Experience in Regulatory Affairs and Labelling
Vishakha Oza has extensive experience in regulatory affairs and project management within the pharmaceutical industry. She worked at Novartis Vaccines from 2009 to 2016 in roles such as Senior Associate in Labelling Regulatory Affairs and Strategic Labelling Specialist in Regulatory Affairs. Her responsibilities included building Company Core Data Sheets (CCDS) and Company Core Safety Information (CCSI). She also worked at Biological E. LTD as Regulatory Affairs Executive Vaccines in Hyderabad, India, from 2007 to 2009.
Expertise in Clinical Trials Safety and Pharmacovigilance
Vishakha Oza possesses a strong background in clinical trials safety and pharmacovigilance. She has worked at GSK as a Safety Scientist in Vaccines SERM, Clinical Safety, and Pharmacovigilance. Additionally, she gained experience at MSN Labs Ltd Hyderabad as a Pharma Research & Development Associate from 2005 to 2007. Her role often involved monitoring and managing drug safety profiles throughout the clinical trial phases.