At Sesh Products US, Inc., the makers of Sesh+, we are dedicated to ensuring the highest regulatory standards and compliance for our products. We’re looking for a detail-oriented Document Control & QMS Specialist who can effectively collaborate with our Operations, Customer Service, Marketing teams, suppliers, and contract manufacturers. This role is integral to our Quality and Compliance Team, where you’ll work closely on regulatory requirements around the Premarket Tobacco Application (PMTA) process, managing documents, maintaining accurate records, and ensuring that our Quality Management System (QMS) aligns with FDA standards for tobacco and nicotine products.
About Sesh Products US, Inc.Sesh Products US, Inc., through our Sesh+ line, is a fast-growing, innovative CPG brand in the nicotine space, committed to delivering safe, compliant, and high-quality products to consumers. Our company champions better, less harmful alternatives and leads with a focus on strict quality and regulatory standards. Joining our team means becoming a vital part of our mission to elevate product safety and regulatory compliance.
SummaryAs the Document Control & QMS Specialist, you will play a critical role in the execution, monitoring, and continuous improvement of our production, quality, and regulatory compliance programs. Reporting to the Director of Compliance, you’ll manage document lifecycles related to our PMTA submissions and ensure all documentation complies with regulatory requirements. This role involves close collaboration with internal and external stakeholders to uphold the integrity of our FDA-compliant QMS.
Key ResponsibilitiesThis is an office-based role, requiring the ability to sit for extended periods.
If you are ready to take on a regulatory-focused role that supports the integrity and safety of Sesh Products US, Inc. and our Sesh+ line, we encourage you to apply. Join us and be part of a team dedicated to upholding excellence in compliance and quality.
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