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Chantecaille is hiring a Regulatory Affairs Specialist to ensure global regulatory compliance and coordinate product registration for its cosmetics portfolio. The role maintains product dossiers, artworks, and registration records, and advises internal stakeholders on regulatory changes and their impacts. Responsibilities Ensures timely and accurate product registration globally Refine and implement registration guid

MANSCAPED is a global men’s grooming and lifestyle consumer brand offering cosmetics, personal care, grooming tools, and related products through omnichannel channels. The Regulatory Affairs Specialist will support global regulatory compliance by managing documentation, registrations, labeling, claims substantiation, monitoring regulations, and providing regulatory guidance across the product lifecycle. Responsibilit

Responsibilities Prepare, review, and maintain regulatory submissions and documentation for medical devices in accordance with applicable FDA requirements Support regulatory compliance activities throughout the medical device product lifecycle Review product documentation, labeling, and technical files for accuracy and compliance with regulatory standards Monitor changes to FDA regulations and other applicable medica

Health Research, Inc. (HRI) Roswell Park Division operates the Clinical Trials Office at Roswell Park Comprehensive Cancer Center. The Regulatory Affairs Specialist ensures investigational product submissions comply with FDA regulations, advises investigators on regulatory requirements, and maintains electronic tracking of FDA submissions. Responsibilities Ensures that Roswell Park IND’s/IDE’s and other regulatory su

OrganOx is a commercial-stage organ technology company developing solutions to improve outcomes for patients with acute or chronic organ failure. The Regulatory Affairs Specialist supports global regulatory submissions, registrations, product lifecycle activities, regulatory information management, and cross-functional coordination for OrganOx medical device products. Responsibilities Support the preparation, compila

Katalyst CRO is seeking a Regulatory Affairs Specialist to support Baxter medical device regulatory activities. The role coordinates and prepares global submissions, reviews technical and scientific data, supports regulatory strategies, responds to regulatory authorities, and maintains documentation for U.S. and international markets, particularly the EU. Responsibilities Support execution of regulatory project plans

Responsibilities The Regulatory Affairs Specialist (RAS) works to gain successful 510k approval by leveraging their skills and expertise to anticipate regulatory requirements and integrate compliance into project plans The RAS streamlines preparation and submissions, by ensuring documentation is accurate, complete, organized and accessible The RAS will work effectively with other departments to compile information an