Devi Niveditha Rajkumar

With a strong background in pharmaceutical quality assurance, GMP compliance, and complaint investigations, I am confident that my experience and skills align closely with Novocol’s commitment to delivering high-quality sterile injectable products and patient-centered value.In my current position as a Release Technician at Baxter International, I perform detailed batch record reviews, approve deviations, and lead NCR investigations within the Trackwise 8 system. Collaborating with production, IT, and quality teams, I ensure that issues are promptly resolved and that all documentation meets regulatory and Health Canada standards. My experience in authoring and reviewing quality documentation, along with training new team members, has strengthened my analytical and leadership abilities.Previously, as a Quality Assurance Associate at Catalent Pharma Solutions, I conducted in-process quality checks, ensured compliance with cGMP and SOPs, and participated in deviation and event investigations. These roles have given me a comprehensive understanding of product quality life cycles, root cause analysis, and corrective and preventive action (CAPA) systems — all integral to effective complaint management.I hold a Master’s in Medical Biotechnology from the University of Windsor, where I gained a solid foundation in analytical techniques and pharmaceutical processes.

With a strong background in pharmaceutical quality assurance, GMP compliance, and complaint investigations, I am confident that my experience and skills align closely with Novocol’s commitment to delivering high-quality sterile injectable products and patient-centered value.In my current position as a Release Technician at Baxter International, I perform detailed batch record reviews, approve deviations, and lead NCR investigations within the Trackwise 8 system. Collaborating with production, IT, and quality teams, I ensure that issues are promptly resolved and that all documentation meets regulatory and Health Canada standards. My experience in authoring and reviewing quality documentation, along with training new team members, has strengthened my analytical and leadership abilities.Previously, as a Quality Assurance Associate at Catalent Pharma Solutions, I conducted in-process quality checks, ensured compliance with cGMP and SOPs, and participated in deviation and event investigations. These roles have given me a comprehensive understanding of product quality life cycles, root cause analysis, and corrective and preventive action (CAPA) systems — all integral to effective complaint management.

I hold a Master’s in Medical Biotechnology from the University of Windsor, where I gained a solid foundation in analytical techniques and pharmaceutical processes.