Viktorija K.

Regulatory Affairs Proficiency: Extensive experience in managing drug registration and compliance processes, including preparation of submissions, interaction with regulatory authorities, and ensuring adherence to international standards. Analytical Skills: Strong ability to analyze complex data, interpret results, and make informed decisions. Proficient in using analytical techniques and instrumentation to ensure product quality and regulatory compliance. Attention to Detail: Meticulous in reviewing and preparing documentation to meet regulatory requirements and maintain high standards of quality assurance. Problem-Solving Abilities: Adept at identifying issues, developing solutions, and implementing corrective actions to address regulatory and quality-related challenges. Communication Skills: Effective communicator with experience in drafting clear and concise reports, interacting with regulatory bodies, and collaborating with cross-functional teams. Process Improvement: Committed to continuous improvement in pharmaceutical processes and quality assurance practices. Proactive in staying updated with industry advancements and regulatory changes. Language Proficiency: Fluent in English (B2), Russian (Native), and Latvian (Native), facilitating effective communication in diverse professional environments. Technical Writing: Skilled in preparing detailed documentation, including Drug Master Files, with accuracy and clarity, ensuring compliance with regulatory standards.