Polytimi Kallergi
Regulatory Affairs Manager at Viatris
Based in Greece
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Seniority
Manager
Department
Manufacturing & Production
Location
Greece
Industry
Pharmaceutical Manufacturing
Company size
18K
Contact information
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p•••••••@viatris.com
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Background
About Polytimi Kallergi
Experienced Regulatory Affairs Manager with nearly 20 years of hands-on involvement in the pharmaceutical industry, combining scientific expertise with strategic regulatory insight. Specializing in regulatory strategy, lifecycle management, and regulatory submissions for branded and generic medicines, medical devices, food supplements, and cosmetics. Proven ability to manage complex regulatory portfolios across EU and international markets, ensuring full compliance while enabling business goals. Key strengths include: End-to-end dossier preparation (CTD/eCTD) and lifecycle submissions Direct communication with Health Authorities (EU, Greece, Cyprus, Malta) Review of Product Information, labeling, and promotional materials Cross-functional collaboration with QA, Medical, Commercial, Supply Chain Leading teams and managing post-merger integrations Proficiency in Veeva Vault, Lorenz Docubridge, Ennov RIMS, SAP
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