Senior Regulatory Manager, Quality
hace 5 días
Senior Regulatory Manager, Quality Join to apply for the Senior Regulatory Manager, Quality role at Fullscript . Founded in ****, Fullscript is a healthcare platform built on the belief that care should treat the whole person. Today, more than 125,000 practitioners and 10 million patients count on us for access to high‑quality supplements, industry‑leading labs, and tools that make it easier to follow through on care. Our purpose is simple: to help people get better. Every system we design and every program we deliver supports practitioners in providing care that is more personal, more efficient, and more effective. This is your invitation. Bring your ideas. Bring your grit. Bring your care for people. Let’s build a healthier future together and make healthcare whole. Role Overview The Senior Regulatory Manager plays a key role in leading regulatory strategy and ensuring compliance across our diverse product ecosystem, from supplements and cosmetics to diagnostic test kits and food products. This position supports regulatory operations spanning FDA, FTC, Health Canada, CFIA, CLIA, and other relevant frameworks, promoting collaboration and continuous improvement across Fullscript's quality system. What You’ll Do Lead and mentor the Regulatory team, fostering a culture of ownership, accountability, and professional growth. Oversee regulatory operations and readiness for audits and inspections across the FDA, FTC, Health Canada, CFIA, CLIA, and other authorities. Manage and maintain regulatory registrations, facility licensing, and supplier qualifications. Partner with internal teams to confirm product labeling and marketing claims across supplements, cosmetics, foods, and diagnostics. Collaborate on complaint handling, recalls, and corrective actions in partnership with Distribution, Finance, Customer Experience, and Brand teams. Work cross‑functionally with Legal, Quality, and Distribution to proactively anticipate regulatory changes and strengthen processes to ensure ongoing improvement and alignment across SOPs and documentation. Provide regulatory oversight for diagnostic laboratories and self‑collection testing kits, ensuring compliance with CLIA and related regulations. Monitor and report on key regulatory KPIs, providing performance insights and recommendations to leadership. What You Bring 10+ years of regulatory compliance experience, including 5+ years in a management role overseeing regulatory professionals. Deep working knowledge of U.S. and Canadian regulations specific to dietary supplements, foods, cosmetics, diagnostics, OTCs, and medical devices. Strong familiarity with FDA, Health Canada, CFIA, CLIA, FTC, and Prop 65 regulations. Experience with cGMP and NSF ***** requirements. Proven ability to lead regulatory strategy, manage audits, and make informed decisions in high‑stakes situations. Bachelor’s degree in a life sciences field (e.g., Food Science, Biology, Biochemistry, Clinical Laboratory Science); advanced degree preferred. Exceptional leadership and communication skills, with the ability to manage and influence cross‑functional stakeholders effectively. Bonus experience: translating complex regulatory requirements into clear guidance for non‑technical stakeholders, implementing or optimizing regulatory software systems or digital quality management tools, navigating ambiguity in evolving regulatory environments, background in supplier or contract manufacturer auditing. Why You’ll Love Fullscript Market competitive compensation package including equity. 401K matching (within US) and RRSP matching (within CAD). Flexible PTO policy. Flexible benefits package and additional perks. Employee discount on Fullscript catalog of products for family & friends. Ability to work wherever you work well. Team Values Values innovation—we push boundaries and always look for better ways. Supports growth—through learning, mentorship, and meaningful work. Cares about balance—with flexible work options and time off when you need it. Fullscript is an equal‑opportunity employer committed to creating an inclusive workplace. Accommodations are available upon request—email ****** for support. Before joining the team, all candidates who receive and accept an offer will complete a background check. We use AI tools to support parts of our hiring process, like screening and reviewing responses. Final decisions are always made by people. This process complies with privacy and employment laws across Canada and the U.S. More Info: SOCIAL: @fullscriptHQ. Let’s make healthcare whole. #J-18808-Ljbffr
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Quality & Regulatory Affairs Manager
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Tigre, Argentina Fullscript A tiempo completoQuality & Regulatory Affairs Manager at Fullscript Founded in ****, Fullscript provides a health intelligence platform that powers every part of care for 125,000 practitioners and supports over 10 million patients. What You’ll Do Maintain ongoing compliance with FDA 21 CFR 111, DSHEA, and NSF ***** for finished dietary supplements. Manage Health Canada...
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Quality & Regulatory Affairs Manager
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Tigre, Argentina Fullscript A tiempo completoQuality & Regulatory Affairs Manager at Fullscript Founded in ****, Fullscript provides a health intelligence platform that powers every part of care for 125,000 practitioners and supports over 10 million patients. What You’ll Do - Maintain ongoing compliance with FDA 21 CFR 111, DSHEA, and NSF ***** for finished dietary supplements. - Manage Health...
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Tigre, Argentina Fullscript A tiempo completoA health intelligence platform provider is seeking a Quality & Regulatory Affairs Manager to ensure compliance with FDA and Health Canada regulations for dietary supplements. Responsibilities include managing licensing and inspections, overseeing supplier qualifications, and contributing to compliance initiatives. The ideal candidate has over 5 years of...
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