NewSenior Medical Science Liaison - Florida Jazz PharmaceuticalsSenior Medical Science Liaison - FloridaTampa, FL$184,000–$276,000 / yearThe successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. See Jazz Pharma Privacy Policy at https://www.icims.com/legal/privacy-notice-website/ and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions.
NewCVN CLINICIAN Aspire Health PartnersCVN CLINICIANTAMPA, FLServing nearly 40,000 clients per year, with locations in six Central Florida counties and currently expanding into Hinesville, Georgia Aspire has delivered state-of-the-art behavioral healthcare and is regularly sought out both statewide and nationally as an expert in the field. With its mission of providing the highest quality of compassionate, comprehensive, and cost effective integrated behavioral healthcare, Aspire, through its more than two dozen campus locations provides a comprehensive continuum of services for children, adolescents, adults, seniors, and families.
NewCVN Licensed Therapist Aspire Health PartnersCVN Licensed TherapistTAMPA, FLServing nearly 40,000 clients per year, with locations in six Central Florida counties and currently expanding into Hinesville, Georgia Aspire has delivered state-of-the-art behavioral healthcare and is regularly sought out both statewide and nationally as an expert in the field. With its mission of providing the highest quality of compassionate, comprehensive, and cost effective integrated behavioral healthcare, Aspire, through its more than two dozen campus locations provides a comprehensive continuum of services for children, adolescents, adults, seniors, and families.
NewLAC GA Policy Strategy and Execution, Senior Director VisaLAC GA Policy Strategy and Execution, Senior DirectorMiami, FL$185,000–$296,100 / yearUnder the direction and in close coordination with the GA LAC SVP, this leader will help build and run the backbone of the LAC Government Affairs function, ensuring that regional priorities, market needs, global alignment, budget and workforce planning, strategic initiatives, reporting, and collaboration mechanisms are coordinated through a high-performing hub model. In coordination with the GA LAC SVP, this leader will partner closely with regional and global Government Affairs leaders, Legal, Product, Compliance, Technology, Strategy, Operations, and Business Functions to align policy positions with Visa’s strategic priorities and enable effective regional execution.
Innovation Strategy Manager GrifolsInnovation Strategy ManagerBoca Raton, FLAs the head of the Plasma Innovation Hub, this role defines strategic innovation priorities, manages high‑impact projects, and drives cross‑functional experimentation that contributes to the transformation of the donor and plasma value chain. Reporting to the Head of Business Development & Plasma Affairs, the Strategy Manager oversees the Innovation vertical and collaborates closely with global stakeholders to ensure initiatives deliver measurable business value and operational improvements.
Regulatory Affairs Associate Illinois Tool WorksRegulatory Affairs AssociateLakeland, FLThis role works closely with Regulatory Affairs, EHS & Quality, R&D, Product Development, Supply Chain, Marketing, and Operations to assess product compliance, maintain regulatory documentation, and support product lifecycle management activities. The Regulatory Affairs Associate supports the organization's product stewardship and regulatory compliance programs by ensuring products meet applicable environmental, health, safety, transportation, and chemical regulatory requirements.
Regulatory Affairs Associate ITWRegulatory Affairs AssociateLakeland, FloridaThis role works closely with Regulatory Affairs, EHS & Quality, R&D, Product Development, Supply Chain, Marketing, and Operations to assess product compliance, maintain regulatory documentation, and support product lifecycle management activities. The Regulatory Affairs Associate supports the organization's product stewardship and regulatory compliance programs by ensuring products meet applicable environmental, health, safety, transportation, and chemical regulatory requirements.
Compliance Manager, Licensing & Regulatory Affairs Felix TechnologiesCompliance Manager, Licensing & Regulatory AffairsMiami, FloridaWe are a hyper-growth Series C company, backed by over $200 million in funding from top-tier global investors, including QED, Castle Island, Switch Ventures, HTwenty, Monashees, and Andreessen Horowitz with support from General Catalyst Customer Value Fund. This individual will own the day-to-day management of Felix’s licensing portfolio, support expansion into new jurisdictions and products, and serve as the primary coordinator for regulator communications, examinations, and licensing-related projects.
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.
Manager, Regulatory Affairs OpenworkManager, Regulatory AffairsBoca Raton, FLORIDAAssess accuracy and completeness of submission documents throughout product lifecycle, specifically pre-application submissions (e.g., meeting requests), new application submissions (e.g., Investigational New Drug applications [IND], Biological License Applications [BLA], Orphan Drug applications [OD]), maintenance submissions (e.g., end-of-phase reports, annual reports, changes to IND or BLA Common technical Document [CTD] dossier, safety reports, product license renewals, establishment license renewals, meeting requests) and post-marketing submissions (e.g., annual reports, periodic safety reports, annual reports of Post-marketing requirements or commitments), and other related documents or submissions. Determines regulatory strategy that aligns with business strategy, defines submission requirements and coordinates the collection of required data, information, and documentation from pertinent departments, facilities, and affiliates, and from contractors/vendors as needed.
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.
Licensing & Regulatory Affairs Analyst III Banco InterLicensing & Regulatory Affairs Analyst IIIMiami, FL5 years of experience in MSB licensing, regulatory compliance, or regulatory affairs within a U.S. financial institution, MSB, fintech, or payments company. As pioneers, we transformed the market by launching Brazil's first digital bank and continue to shape the future with cutting-edge technology.
Senior Manager, Regulatory Affairs OpenworkSenior Manager, Regulatory AffairsBoca Raton, FLORIDAResponsible for the preparation, review, presentation, and publishing of all FDA submissions to assure accuracy and completeness of submission documents, which includes but is not limited to meeting requests/briefing packages and presentations to the FDA (e.g., preIND/pre-BLA, end-of-phase II, Type A, B or C, and advisory committee meetings), Investigational New Drug Applications (INDs), Biologic License Applications (BLAs), Orphan Drug Applications, Marketing and Promotional Materials, Product Listing and Establishment License Applications, and other related documents or CMC supplement submissions. Provides accurate and timely regulatory guidance to Management, Process Development, Analytical Development, Manufacturing, and the Quality Assurance/Quality Control staff while maintaining frequent contact with the Head of Regulatory Affairs.
Senior Director, Regulatory Affairs (Inhalations – ANDAs and 505 (b)(2)) Lupin Pharmaceuticals Inc.Senior Director, Regulatory Affairs (Inhalations – ANDAs and 505 (b)(2))Coral Springs, FloridaResponsibilities: The Senior Director of Regulatory Affairs is responsible for establishing regulatory direction and providing management support for the US development of complex Inhalation products within Lupin’s complex portfolio, with a robust execution skill set. Somerset, New Jersey is home to one of Fifteen commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, as well as additional Research and Development teams.
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.
LICENSING & REGULATORY AFFAIRS ANALYST III Banco Inter SALICENSING & REGULATORY AFFAIRS ANALYST IIIMiami, FL5 years of experience in MSB licensing, regulatory compliance, or regulatory affairs within a U.S. financial institution, MSB, fintech, or payments company. As pioneers, we transformed the market by launching Brazil's first digital bank and continue to shape the future with cutting-edge technology.
NewRegulatory Affairs Manager Aso LLCRegulatory Affairs ManagerSarasota, FLThe Regulatory Affairs Manager will be responsible for leading ASO's Regulatory and Compliance directives carrying out a wide range of initiatives while ensuring compliance to FDA and other regulatory bodies/entities in addition ensuring adherence to the Quality Management System. Develops and maintains regulatory network (formal and informal) by establishing relationships with various regulatory bodies, local consultants and legal entities within the respective countries / regions where ASO has.
Senior Manager Regulatory Affairs SyncromuneSenior Manager Regulatory AffairsFort Lauderdale, FL$160,000–$180,000 / yearFinal determinations with respect to salary will take into account a number of factors, which may include, but not be limited to, the primary work location and the chosen candidate’s relevant skills, experience, and education. The Senior Manager of Regulatory Affairs will assist in all facets of the company’s Regulatory Affairs for all U.S. and international regulatory matters, including filings and interactions with regulatory authorities.
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.
LICENSING & REGULATORY AFFAIRS ANALYST III Inter CarreirasLICENSING & REGULATORY AFFAIRS ANALYST IIIMiami, FLGet to Know Inter • As pioneers, we transformed the market by launching Brazil’s first digital bank and continue to shape the future with cutting-edge technology.• Conheça o Inter Pioneiros, mudamos o mercado ao lançar o primeiro banco digital do Brasil e seguimos criando tendências com tecnologia de ponta.