Our Team – UNIVITA

The Managing Director of Univita Limited brings over 20 years of experience in marketing and business development across the CIS region, with expertise in executive leadership, client strategy, regulatory affairs, commercial growth, and operational oversight. The role is focused on regulatory affairs, market access, manufacturing strategy, and commercialization within the pharmaceutical sector.

Managing Director

Sanjay Kumar

An Enterprising Leader with chronicled success & international experience of over 30 years in spearheading the entire Business & Operational Excellence, Strategy, Concept Evolution, Business Set-up and Project Establishment, Product Registration, QMS and R&D across multi-functional departments; leveraged capabilities in conceptualizing & implementing effective ideas / strategies which adds value to organization through inspiring leadership, rich experience & innovation excellence; targeting to express potential in leadership roles with an esteemed organization.

Technical adviser, Project Management, Business development

Dr. Sanjeev Kolhe

A result-driven management professional with over 28 years of experience in Project Planning Project Execution, Plant Operation, Documentation and People Management. Our expert has served industries such as pharmaceuticals, API, biotech, R&D labs, food, cosmetics and logistics. Our projects adhere to global standards like US FDA, WHO-GMP, EU GMP, PICs, MHRA, TGA, and Schedule M, ensuring compliance and operational efficiency from concept to commissioning.

Projects & Engineering

Amrendra Kumar Singh

Our expert has over 25 years of extensive experience in the pharmaceutical sector, specializing in both non-sterile and sterile formulations. His expertise spans Quality Assurance (QA), Quality Control (QC), plant operations, and project management, including greenfield projects as well as plant modification and expansion initiatives. He has worked with multinational corporations and internationally based companies across the US, Europe, CIS, and ASEAN regions, ensuring compliance with global regulatory standards such as US FDA, WHO-GMP, EU GMP, EAEU, PIC/S, MHRA, TGA, ANVISA, and Schedule M. He has successfully conducted more than 250 GxP audits worldwide, covering GMP, GLP, GDP, cosmetics, biological products, and fermentation-based, medical devices products.

Quality, Operations and Audits

Vikaskumar Javle

Our expert is Regulatory Head and PIC-S (Ukraine) Inspection Expert in the pharmaceutical industry involves ensuring regulatory compliance, managing interactions with health authorities, and supporting GMP inspection readiness in line with international standards.

Regulatory Head – CIS Region

Hennadii Vorona

The Admin and HR Head is responsible for overseeing human resources management, administrative operations, organizational policies, and employee engagement to ensure efficient business operations and workforce effectiveness.

Admin & HR Head

Zhanna Aksenko

Subir Narayan specializes in IT governance, cyber security, and structured technology operations for regulated and compliance-driven environments. His expertise includes audit-ready IT infrastructure, disaster recovery governance, access management, cyber risk reduction, endpoint governance, and SOP-oriented operational frameworks. As a Technology Advisor, he supports organizations in strengthening operational resilience, documentation maturity, and governance-aligned technology practices across pharmaceutical and regulated business ecosystems. His focus is on enabling secure, compliant, and scalable technology environments aligned with operational continuity, accountability, and audit readiness.

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