Deven Nahar
About Deven Nahar
Deven Nahar is the Manager of Submissions Operations Management for EMEA at BeiGene, with a background in regulatory operations and pharmacology.
Current Role at BeiGene
Deven Nahar is currently the Manager of Submissions Operations Management for the EMEA region at BeiGene. He started this role on June 1, 2021. His responsibilities include overseeing submissions operations, ensuring compliance with regulatory requirements, and coordinating between different regional teams to facilitate smooth submissions processes.
Previous Experience at Jazz Pharmaceuticals
Between 2018 and 2021, Deven Nahar worked as a Senior Associate Regulatory Operations at Jazz Pharmaceuticals in Oxford, United Kingdom. During his tenure, he managed regulatory submissions and contributed to the company's compliance with global standards. His role involved complex document management and coordination with multiple stakeholders.
Professional Journey at Pfizer
Deven Nahar has had two stints at Pfizer. From 2015 to 2018, he worked as a Regional Regulatory Hub Strategist, where he strategized regional regulatory submissions and ensured alignment with regulatory standards. Prior to that, he held the position of Hub Submission Manager from 2014 to 2015 in Sandwich, Kent, United Kingdom, focusing on managing and coordinating submission processes.
Academic Background in Pharmacological Sciences
Deven Nahar studied at Coventry University, earning a degree in Medical and Pharmacological Sciences from 2009 to 2012. During his academic tenure, he developed essential skills in project management, communication, and complex research, which have been crucial in his regulatory roles within the pharmaceutical industry.
Early Career and Roles at Hospira and Pinnaculum Limited
In his early career, Deven Nahar worked as a Labelling Administrator at Hospira from 2013 to 2014 in Royal Leamington Spa, Warwickshire, UK. Shortly before that, he served as a Pack Management Planner at Pinnaculum Limited in 2013. These roles helped him gain valuable experience in administrative processes and project management in the pharmaceutical industry.