Krantiveer Singh
Regulatory Affairs Assistant @Give and Go Prepared Foods
Signup · Get unlimited contacts
WORK HISTORY
Regulatory Affairs Assistant @Give and Go Prepared Foods
Toronto, ON, CA
Give and Go Prepared Foods, viz, part of Mondelēz International.• Ensure regulatory compliance for ingredients, formulations, labeling, and packaging across Canada, the USA, and international markets, supporting timely product launches.• Lead supplier and ingredient approval processes, ensuring allergen, nutritional, and certification compliance.• Drive the successful removal of Red3 from product formulations, enhancing ingredient safety and regulatory compliance.• Monitor regulatory updates and provide expert guidance to cross-functional teams, mitigating risks and enabling compliant marketing.
EDUCATION
Guru Nanak Dev University, Amritsar
Bachelor of Science, Life Sciences
Guru Nanak Dev University, Amritsar
Master of Science, Human/Medical Genetics
Northeastern University
Master of Science - MS, Regulatory Affairs of Drugs, Biologics & Medical Devices
ABOUT KRANTIVEER SINGH
Regulatory Affairs professional with a multidisciplinary background in Human Genetics and Regulatory Affairs, supporting regulatory compliance, documentation, and lifecycle activities across pharmaceuticals and other regulated healthcare product categories.I bring experience supporting Health Canada and FDA–aligned regulatory frameworks across Canadian, U.S, and international markets, with hands-on involvement in product classification, formulation and ingredient assessments, labeling and claims review, and maintenance of high-quality regulatory documentation. My work emphasizes scientific rigor, regulatory accuracy, and inspection-ready records throughout product development and post-market phases.I hold an M.Sc. in Human Genetics and a Master of Science in Regulatory Affairs from Northeastern University. This combined training allows me to interpret complex scientific data, assess regulatory risk, and translate evolving regulatory requirements into clear, actionable guidance for cross-functional teams.I collaborate closely with R&D, Quality Assurance, Marketing, and Supply Chain partners to support compliant decision-making across the product lifecycle from early development through commercialization and ongoing change management. I am particularly interested in regulatory roles that span pharmaceutical development, lifecycle management, and global regulatory compliance within dynamic, science-driven organizations.
This profile is compiled from publicly available professional sources. Unifers is not affiliated with or endorsed by LinkedIn. Request removal of this profile.