Are you passionate about ensuring regulatory compliance and navigating the complexities of regulatory frameworks? Do you want to play a key role in gaining approvals for new drugs while safeguarding patient safety? If so, we are looking for a dedicated Regulatory Affairs Specialist to join our team in Uzbekistan or Kazakhstan. Your new role In the role of Regulatory Affairs Specialist, you will facilitate the registration of new medicines and cover Uzbekistan, Georgia, Mongolia, Turkmenistan. Your main responsibilities will be: <ul style="margin-bottom:8.0pt;margin-top:0.0px"> <li style="margin:0.0cm 0.0cm 8.0pt 0.4px;line-height:107%;background-color:white;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Lead end-to-end regulatory activities (registration, renewals, variations, and lifecycle management) for products, ensuring full compliance with local and international regulations.</li> <li style="margin:0.0cm 0.0cm 8.0pt 0.4px;line-height:107%;background-color:white;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Prepare and coordinate submission documentation, including local normative documents, with alignment and approval from Headquarters (HQ).</li> <li style="margin:0.0cm 0.0cm 8.0pt 0.4px;line-height:107%;background-color:white;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Manage labeling activities: develop mock-ups and package leaflets (including Russian/local language versions) and submit artwork/labeling cases via corporate systems.</li> <li style="margin:0.0cm 0.0cm 8.0pt 0.4px;line-height:107%;background-color:white;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Liaise with Health Authorities: prepare responses to queries and deficiency letters, coordinate with HQ, and manage translation and submission of required documents.</li> <li style="margin:0.0cm 0.0cm 8.0pt 0.4px;line-height:107%;background-color:white;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Maintain accurate and timely updates in global systems (e.g., RIM, Vault, novoGloW) to ensure proper tracking of registration status.</li> <li style="margin:0.0cm 0.0cm 8.0pt 0.4px;line-height:107%;background-color:white;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Monitor regulatory changes and provide guidance to internal stakeholders and HQ, supporting submission planning and special projects.</li> <li style="margin:0.0cm 0.0cm 8.0pt 0.4px;line-height:107%;background-color:white;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Collaborate cross-functionally (HQ, local teams, vendors) to ensure compliance, approval of promotional materials, and adherence to Quality, Pharmacovigilance, and QMS requirements.</li> </ul> Your new department Novo Nordisk Representative offices in Uzbekistan or Kazakhstan, based in Tashkent or Almaty. You will work closely with marketing, sales and medical colleagues and benefit from strong collaboration with the wider regional RA community. Your skills & qualifications We are looking for a candidate with the following qualifications: <ul style="margin-bottom:0.0cm;margin-top:0.0px"> <li style="margin:0.0cm 0.0cm 0.0cm 0.4px;line-height:14.0pt;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Bachelor’s degree in pharmacology, Chemical or Healthcare</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.4px;line-height:14.0pt;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Minimum 1 year of experience in similar position</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.4px;line-height:14.0pt;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Knowledge of regulatory environment and local legislation</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.4px;line-height:14.0pt;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Experience with safety updates, labelling variations, regulatory submissions, and use of local regulatory IT systems</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.4px;line-height:14.0pt;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Good communication, negotiation, and time‑management skills to support cross‑functional collaboration under tight deadlines</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.4px;line-height:14.0pt;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">Confident PC and IT systems user (incl. Microsoft and others)</li> <li style="margin:0.0cm 0.0cm 2.0pt 0.4px;line-height:14.0pt;font-size:10.0pt;font-family:arial, helvetica, sans-serif;color:black;text-indent:0.4px">English language skills (both written and spoken)</li> </ul> Working at Novo Nordisk Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results. Deadline 03.07.2026. Applications are reviewed on an ongoing basis. Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process. Novo Nordisk is not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

Regulatory Affairs Specialist (Tashkent, Tashkent, UZ) @ novonord

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