Responsibilities: Preparing documentation for international regulatory registrations. Preparing technical documentation to comply with MDD and EU MDR. Defining worldwide regulatory requirements necessary for regulatory approval of products. Participating in cross functional teams as regulatory lead. Maintaining regulatory documentation to ensure availability for external audits.
...We provide care for more than 120,000 patients, most of which are beneficiaries of government-sponsored healthcare programs like Medicare, or of health plans purchased on the Affordable Care Act exchange marketplace. MaxHealth is a rapidly growing medical practice with...
...of niche sales and service strategies to achieve business growth objectives. Reports Directly & Functionally To: Vice President/General Manager Direct Reports includes: Customer Account Leaders, Customer Service Administrators and Customer Service Engineers...
...Title: Creative Copywriter Location: Stamford, CT - Hybrid (4 days onsite, 1 remote) Pay Rate: $45-55/hr Must-Haves: ~5+ years of proven experience as a copywriter, with a strong portfolio showcasing conceptual thinking and successful entertainment-focused...
...more humane. We believe that AI will fundamentally transform how people work. In the future, everyone will work in tandem with expert AI... ...synthesize information, and execute work. These assistants will free people up to focus on the higher-level, creative aspects of...
...staff. Maintain and submit documentation as required by the Company and/or facility. Prepare and submit timely written reports of... ...standards of professional conduct in relation to information that is confidential in nature. Share information only when the recipient's right...