Senior Scientific and Regulatory Manager (BB-900A1)

Found in: Talent CA

Senior Scientific and Regulatory Manager Intertek Scientific and Regulatory Consultancy Group is looking for a motivated and client focused senior scientist and regulatory affairs professional who is seeking an opportunity to contribute to the excellence and growth of our food, nutrition and regulatory consulting services. The Senior Scientific and Regulatory Manager will use their scientific expertise and strong project management skills to guide our clients on matters related to food ingredient compliance, regulations, guidance, and applicable statutes related to global food ingredient approvals. This role combines knowledge of global regulatory affairs with a deep understanding of toxicology and general risk assessment practices for food ingredients/additives. Responsibilities: Analyse and critically assess scientific issues and prepare professional quality reports which interpret and summarize these issues, acting as a senior scientific leader for the team. Establish and maintain regulatory relationships with key clients as well as internal and government stakeholders, to promote Intertek’s mission and values of total quality assurance and scientific excellence. Effectively utilize established network of contacts within the industry, including trade associations, consultants and regulatory agency contacts, to identify and resolve regulatory issues and increase visibility to our expertise and services. Act as key account contact, project manager, and author/reviewer of submission documents, utilizing strong track record of regulatory success bringing GRAS/novel food ingredients to the market on time and on budget. Lead successful project teams, applying effective organizational and planning skills required in a multidisciplinary and matrixed environment. Desired qualifications: B.S., M.S., Ph.D., or JD in regulatory science, regulatory law or risk assessment, toxicology, cellular or molecular biology, fermentation science, or combination thereof. 5-10 years of experience working in the regulatory sciences within the food manufacturing industry. Strong knowledge of the U.S. regulatory system required and general understanding of EU and Canadian regulatory systems desirable. Subject matter expertise in FDA food safety frameworks; demonstrable success in designing and implementing evidence-based risk assessment frameworks for food ingredient safety evaluation; extensive experience in sourcing and applying legal, regulatory, and policy precedents to novel food products; experience leading preparation of GRAS dossiers, EU/Canada novel food applications, food additive petitions, and dietary supplement ingredient notifications. Strong networking skills. Personal characteristics: Excellent oral and written communication skills. Well organized and structured (attention to detail). Able to work independently and in teams. Ability to work remotely (home based) or in an office in Mississauga, Ontario. Intertek Canada offers a salary and benefit package competitively placed with the local market. We promote a culture where motivated customer-oriented employees can flourish, experience professional fulfillment and reach their highest potential. Medical, Prescription, Dental, Vision, and Disability Insurance plans; RRSP plan with company match; paid time off (vacation; sick holiday); Employee Assistance Program (EAP); Tuition Reimbursement, and more. #LI-JC1Primary Location:CA-ON-MississaugaWork Locations:Mississauga Argentia Road2233 Argentia RoadSuite 111MississaugaL5N 2X7Job:Professional SciencesOrganization:CAN06:Intertek Health Sciences IncSchedule:RegularEmployee Status:Manager without Direct ReportsFull-timeJob Level:First ShiftTravel:Yes, 15 % of the TimeJob Posting:01.Mar.2021, 3:00:49 PM

calendar_today3 days ago


info Full-time

location_on Mississauga, Canada

work Intertek

I expressly authorise the Terms and Conditions

Similar jobs