Job Description

• Bachelor’s degree or above in Pharmacy, Life Sciences, or related field.
• Minimum 3–5 years of experience in pharmaceutical regulatory affairs, with proven local registration experience in Russia.
• Fluent in English and Russian.
• Strong understanding of Russian regulatory systems and procedures.
• Established relationships with local regulatory authorities or government agencies preferred.
• Excellent communication, negotiation, and problem-solving skills. - Lead and coordinate regulatory submissions and product registration processes in Russia and other assigned international markets.
• Maintain up-to-date knowledge of local and international regulatory requirements, guidelines, and policies.
• Establish and maintain effective communication with Russian health authorities and other relevant government bodies.
• Prepare, review, and submit documentation for new product approvals, renewals, and variations.
• Collaborate closely with R&D, Quality, and Commercial teams to ensure compliance across the product lifecycle.
• Provide regulatory strategy and support for new product launches and market expansion initiatives.

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