Regulatory Affairs Specialist I - Spine Arthrex IncRegulatory Affairs Specialist I - SpineNaples, FLIn coordination with management of Regulatory Affairs, this role will develop regulatory strategy, execute the regulatory plan, and perform other activities that lead to and maintain regulatory approval/clearance/licensure for Arthrex's medical devices. The RA Specialist I - Spine is responsible for managing specific aspects of the Arthrex Regulatory Affairs program with an emphasis on gaining regional regulatory approval/clearance/licensure for medical devices in the most efficient, compliant manner.
Senior Regulatory Affairs Specialist - Clinical MinimedSenior Regulatory Affairs Specialist - ClinicalVirtual, FLRemote$97,000–$165,000 / yearIf you are applying to perform work for MiniMed in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which MiniMed reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Manage projects assigned to support business unit Regulatory Affairs Specialists (RAS) and international regulatory staff to provide regulatory support for new products/therapies and changes to existing products that require clinical evidence.
Sr. Regulatory Affairs Specialist II Treace Medical Concepts IncSr. Regulatory Affairs Specialist IIPonte Vedra, FLAuthors US FDA premarket submissions (e.g., 510(k), Q-submissions) and international submissions with collaboration from key staff in Product Development, Operations, Marketing, and Quality for timely submissions. Supports the Unique Device Identifier (UDI) requirements including US FDA Global Unique Device Identification Database (GUDID) and international UDI submissions.
Principal Regulatory Affairs Specialist- Georgia FloodGate MedicalPrincipal Regulatory Affairs Specialist- GeorgiaTampa, FloridaThe Principal Regulatory Affairs Specialist will serve as the company's lead regulatory execution expert and will be responsible for developing and executing regulatory strategies that support product development, FDA submissions, and global market access. Our flagship product, the ZywieNano MCT Patch — the smallest cardiac monitoring patch on the market — delivers up to 30 days of continuous ECG monitoring paired with ZywieAI, our proprietary AI-driven arrhythmia detection platform.
Senior Regulatory Affairs Specialist - Clinical Medtronic MiniMed IncSenior Regulatory Affairs Specialist - ClinicalFLRemote$97,000–$165,000 / yearIf you are applying to perform work for MiniMed in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which MiniMed reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Manage projects assigned to support business unit Regulatory Affairs Specialists (RAS) and international regulatory staff to provide regulatory support for new products/therapies and changes to existing products that require clinical evidence.
Senior Regulatory Affairs Specialist 26H111 Siemens AGSenior Regulatory Affairs Specialist 26H111Orlando, FLExperience level Experienced Professional Job type Full-time Work mode Hybrid (Remote/Office) Employment type Permanent Any Siemens location in Japan MissionResponsibilitiesPMDAQMS/GVPGlobal RASDSImportant Notice, Pink NoteDCPerformanceCoachingOpportunityTeam CulturePMDA Requirements5 PMDAPreferred)IVDQMSQMSGVPREQ: 26H111 =========================3900173012:0013:004811112(5/1) (12/29-1/4)(6)(5)/ =========================Siemens HealthineersDI&B Job ID 518326 Posted since 18-Aug-2026 Organization Siemens Healthineers Field of work Quality Management Company Siemens Healthcare Diagnostics K.K. Experience level Experienced Professional Job type Full-time Work mode Hybrid (Remote/Office) Employment type Permanent Any Siemens location in Japan MissionResponsibilitiesPMDAQMS/GVPGlobal RASDSImportant Notice, Pink NoteDCPerformanceCoachingOpportunityTeam CulturePMDA Requirements5 PMDAPreferred)IVDQMSQMSGVPREQ: 26H111 =========================3900173012:0013:004811112(5/1) (12/29-1/4)(6)(5)/ =========================Siemens HealthineersDI&B.
Senior Specialist, Regulatory Affairs - International (EMEA) Arthrex IncSenior Specialist, Regulatory Affairs - International (EMEA)Naples, FLCoordinate with Engineering, R&D, Manufacturing, Quality Assurance, and other applicable departments to collect technical information and data associated with the preparation of international regulatory documents to support Arthrex subsidiaries and distributors new product registrations, license renewals, re-registrations, design change notifications, manufacturing and labeling changes, customs requests and international marketing bid/tenders. Essential Duties and Responsibilities: Research and respond to inquiries from Arthrex subsidiaries and distributors to facilitate new product registrations, license renewals, re-registrations, design change notifications, manufacturing and labeling changes, customs requests, international marketing bid/tenders and to support quality tasks related to foreign manufacturer registrations.
Regulatory Affairs Specialist, EHS, North America Henry ScheinRegulatory Affairs Specialist, EHS, North AmericaFloridaDevelop and deliver employee environmental, health, and safety (EHS) awareness and training programs to ensure compliance with applicable federal, state, and international regulations, including OSHA, OSHA State Plans (e.g., Cal/OSHA), DOT, IATA, IMO, and EPA requirements. Proficient in Microsoft Office applications, including PowerPoint, and experienced with project management methodologies and tools commonly used in the medical device or pharmaceutical industries.
Regulatory Affairs Specialist Sunrise Pharmaceutical IncRegulatory Affairs SpecialistSunrise, FLCalibrate and troubleshoot analytical instruments, including pH meters, dissolution apparatus, high-performance liquid chromatography (HPLC) systems, and UV spectrophotometers. Provide regulatory guidance, written reports, and verbal presentations on analytical data, methods, and interpretations to other departments.
Regulatory Affairs Expert - Remote YO AI LabsRegulatory Affairs Expert - RemoteMiami, FloridaRemoteThe role involves assessing clinical documents, ensuring compliance with regulatory guidelines, identifying inconsistencies, and providing clear, evidence-based feedback to improve AI-generated regulatory content. We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating regulatory documentation.
NewSummer 2027 Internship - RA/QA - Post Market Regulatory Affairs - Virtual StrykerSummer 2027 Internship - RA/QA - Post Market Regulatory Affairs - VirtualFloridaHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Currently pursuing a Bachelor’s or Master’s degree in a scientific or technical discipline (e.g., Biomedical Engineering, Biological Sciences, Chemistry, Software Engineering, or related fields) and must remain enrolled in a degree-seeking program after the internship.
Student Affairs and Career Services Specialist (Tampa Campus) National Louis UniversityStudent Affairs and Career Services Specialist (Tampa Campus)Tampa, FL$47,365.13–$66,311.19 / yearManage assigned communications channels to include inboxes, webpages, and social media; Respond in a timely manner (1-2 business days) to inquiries and make referrals to relevant campus supports as needed; Assist in planning, coordinating, and executing new student orientation programs and other events; Prepare communications for relevant student policies, alerts, programming or events. Coordinate student-oriented events including partnering with program chairs and advisors to plan residency weekends and orientations, serve as point-person for Commencement and the Commencement Committee, and partner with the NLU Social Media Manager to coordinate social media posts regarding events.
Digital Affairs & DPO Senior Specialist NubankDigital Affairs & DPO Senior SpecialistMiami, FloridaDemonstrated track record of leading complex privacy and/or AI matters end‑to‑end , such as: Launching or significantly redesigning data‑intensive products under US and international privacy rules; Implementing or maturing a privacy governance or AI governance framework; Leading or advising on complex data or AI incidents and regulatory interactions. Own or co‑own key pillars of the Privacy Governance Program as they relate to the US and global scope, including: Record of Processing Activities (RoPA) and personal data mapping; Privacy and data protection risk management and controls; DPIAs/PIAs and other privacy risk assessments at scale; Global data subject rights (DSR) strategy and processes; Training, awareness and privacy metrics.
NewSUPERVISORY PUBLIC AFFAIRS SPECIALIST United States Air ForceSUPERVISORY PUBLIC AFFAIRS SPECIALISTFL$125,776–$163,514 / yearExamples of specialized experience includes knowledge of providing oversight for activities assigned to the Production Branch, Command Information Division, Secretary of the Air Force Public Affairs Directorate which includes the elements of internal information, visual information, communication planning, social media, media relations, community/Congressional relations, contingency/crisis response, special event planning, security and policy review, and Public Affairs resource management. The mission of US Central Command (USCENTCOM) is: With national and international partners, USCENTCOM promotes cooperation among nations, responds to crises, deters or defeats state and non-state aggression, and supports development and when necessary, reconstruction in order to establish the conditions for regional security, stability and prosperity.
Sr Spec Medical Affairs CordisSr Spec Medical AffairsFloridaFull timeMedical Affairs Specialist will support cross-functional and cross-regional alignment of medical operations and deliverables ensuring strong local execution of global strategy and contributing to operational improvements that enhance internal collaboration, data collection, and compliance. Act as the point of contact for the assigned region for internal stakeholders and identify areas of support in aspects of key product launches, handling off label queries, unsolicited KOL queries and communicate insights to global Medical Affairs leadership.
Medical Affairs Director PBI-Gordon CompaniesMedical Affairs DirectorPensacola, FLThis role supports our mission to empower commercial teams and veterinary clients through expert education, evidence-based insights, and collaborative communication-enabling confident, informed decision-making that elevates patient care within the veterinary specialty pharmaceutical market. If you're energized by clinical leadership in veterinary industry, shaping product strategy across commercialized portfolios and development pipelines, and partnering with cross-functional teams to drive impact, we'd love to hear from you.
REGULATORY SPECIALIST III - 79000149 Government of FloridaREGULATORY SPECIALIST III - 79000149TAMPA, FL$1,396.82–$1,531.54 / weekOur Organization and Mission: The Florida Division of Alcoholic Beverages and Tobacco licenses the manufacture, distribution, sale, and service of alcoholic beverage and tobacco products in Florida, including receipt and processing of license applications; collection and auditing of taxes and fees paid by licensees; and enforcement of the laws and regulation of the alcoholic beverage and tobacco industries, pursuant to Chapters 210, 561-565, 567-569, Florida Statutes. Ability to communicate effectively, both orally and in writing, by understanding written sentences and paragraphs in work related documents, by talking with others to effectively convey information, by actively listening to others, and by communicating effectively with others in writing as indicated by the needs of the audience.
REGULATORY SPECIALIST II - 79011362 Government of FloridaREGULATORY SPECIALIST II - 79011362TALLAHASSEE, FL$1,365.38–$1,390.24 / weekThis position is responsible for performing regulatory administrative duties pertaining to answering phones and handling inquiries from the public, field offices and other state agencies, independently reviewing and researching incoming complex plan review applications for completeness prior to profiling into Versa: Regulation; ensuring proper protocols are followed for check handling and processing; opening, sorting, and delivery of incoming division mail; ensuring temporary event receipt books are processed and temporary event receipt books database is accurately maintained; ensuring emergency closure documentation is processed with expediency and accuracy. Ability to understand and apply applicable rules, regulations, policies and procedures; deal with the public in a tactful and courteous manner; plan, organize, and coordinate work assignments; perform data collection, word processing, email, licensing, internet applications and other technology required by the department, including but not limited to Versa: Regulation and OnBase.
Sr. Research Regulatory Specialist (Full Time, Days) Nicklaus Children's HospitalSr. Research Regulatory Specialist (Full Time, Days)Miami, FLThis position also applies experience using a clinical trial management system (CTMS) and electronic regulatory systems for protocol and regulatory document management, with responsibility for creating, maintaining, and scheduling portfolio reports that keep key stakeholders informed of study progress, regulatory milestones, risks, and overall portfolio status. The Senior Research Regulatory Specialist applies advanced experience supporting Phase 1 research, Independent Review Board (IRB), Institutional Biosafety Committee (IBC) submissions, and a broad range of institutional research committee reviews to guide complex study activation and ongoing regulatory maintenance.
Sr. Regulatory Specialist - Cancer Institutute(Full Time, Days) Nicklaus Children's HospitalSr. Regulatory Specialist - Cancer Institutute(Full Time, Days)Miami, FLThis position also applies experience using a clinical trial management system (CTMS) and electronic regulatory systems for protocol and regulatory document management, with responsibility for creating, maintaining, and scheduling portfolio reports that keep key stakeholders informed of study progress, regulatory milestones, risks, and overall portfolio status. The Senior Research Regulatory Specialist applies advanced experience supporting Phase 1 research, Independent Review Board (IRB), Institutional Biosafety Committee (IBC) submissions, and a broad range of institutional research committee reviews to guide complex study activation and ongoing regulatory maintenance.