Regulatory Affairs Specialist
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A proactive and result-driven professional with more than 5 years of holistic knowledge and hands on expertise in regulatory processes and compliance, new product registrations, global and local clinical trials, and life cycle management and artwork management activities for vaccines, biologicals, pharmaceuticals, food, and cosmetics.
More than 5 years of experience in a multi-national within the regulatory affairs vertical. Competent in project management, mentoring, regulatory intelligence, labelling compliance, strategic planning, lifecycle management activities like NDS, SNDS, CTA, post approval changes, safety reports etc. Well versed in Veeva Vault, G suite, and Microsoft tools.
Post graduate certification in Regulatory Affairs
