Siddharth Tiwari

WORK HISTORY

EDUCATION

ABOUT SIDDHARTH TIWARI

Policy, Quality, Compliance, and License management professional with a strong background and broad skillset derived from experience in developing, implementing, and evaluating policies and procedures. Flexible, innovative, and multitasking team player with strong team management skills. Experienced in handling multiple quality assurance projects among different branches of the organization. Responsible for overviewing various policies and procedures to comply with different Acts and regulations. Demonstrated ability in managing audit and information requests from Health Canada about Compliance, Quality Assurance, and Quality Control. Performed responsibilities for maintaining, updating SOPs, production batch records, and quality management system • Help licence holders in application submission under CTLS- micro and standard cultivation and processing, inlcuding sales licence. • SOP writing, submissions and helping licence holders in obtaining licences • Responsible to review as regulations changed from time to time and updating policies and procedures about the Marihuana for Medical Purposes Regulations (MMPR), Access to Cannabis for Medical Purposes Regulations (ACMPR), Office of Controlled Drugs and Substances Act (CDSA), and Cannabis Act and its regulations • Review Non-conformance Reports and Corrective Action Reports. Approve finished product specifications for different kinds of products. Responsible for managing procedures and processes about incidents, complaints, deviations, and recalls. • Responsible for providing technical guidance to the Operations team among different subsidiary companies for compliance and GPP purposes based on Health Canada requirements. • Communicating and planning with Health Canada inspectors, stakeholders, and technical authorities on matters of regulatory compliance and quality issues. • Developing and applying standard operating procedures based on government guidelines for the license holder. • Developing and facilitating training to all manufacturing departments regarding regulatory requirements for GPP compliance and to further build knowledge of the organization • Provided administrative support towards quality agreements with all third-party vendors including licensed producers, raw material suppliers, testing labs, and warehouses • Holds Health Canada security clearance under ACMPR and Controlled Drugs and Substances Act