UNKNOWN

ADAPTED_NOW

The position requires strong analytical capabilities and demonstrated experience successfully dealing with regulatory issues, excellent levels of communication and presentation skills to interact with national and sub national government officials and developed skills coordinating multi disciplinary groups to lead projects. Visa is a world leader in payments technology, facilitating transactions between consumers, merchants, financial institutions and government entities across more than 200 countries and territories, dedicated to uplifting everyone, everywhere by being the best way to pay and be paid.

YEAR

<p>Visa has been a proud sponsor of the Olympic Games since 1986. Sport unites people, communities and nations. It enriches people’s lives and creates economic development opportunities. In today’s world, where brand and trust mean so much, the Olympic Games reflect those equities found at Visa — worldwide acceptance, reliability, versatility and leadership. Sponsoring the Olympic Games makes good business sense for Visa and our clients.</p>

Visa

Sr. Director; Regulatory Affairs

Director/Associate Director, Thought Leader Engagement – Head & Neck Oncology The Director/Associate Director of Thought Leader Engagement is a field-based marketing role responsible for developing and leading strategic engagement with Head & Neck Oncology Key Opinion Leaders (KOLs), Medical Experts (MEs), and other key influencers across the United States. The Director/Associate Director reports to the Head of Thought Leader Engagement – Head & Neck Oncology and partners closely with cross-functional leaders across Marketing, Sales, Market Access, and Medical Affairs to shape and execute thought leader engagement strategies that support successful launch preparation and execution.

Genmab

Director, Thought Leader Engagement (H&N) - Southeast

Capital Markets Placement_feed

Lennar is one of the nation's leading homebuilders, dedicated to making an impact and creating an extraordinary experience for their Homeowners, Communities, and Associates by building quality homes and providing exceptional customer service, giving back to the communities in which we work and live in, and fostering a culture of opportunity and growth for our Associates throughout their career. The Chief Compliance Officer reports to the Chief Risk & Legal Officer and leads a team of compliance professionals responsible for monitoring, testing, licensing, training, regulatory change management, fair lending, advertising compliance, and other compliance advisory functions.

Lennar Corporation

Chief Compliance Officer

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.

Lupin Pharmaceuticals Inc.

Senior Director, Regulatory Affairs (Inhalations – ANDAs and 505 (b)(2))

Lupin Somerset Jobs

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You will engage with federal and state policymakers, regulatory commissions, economic development authorities, and industry stakeholders to anticipate policy shifts and advocate for outcomes that accelerate interconnection, support large-load energy development, and enable competitive data center growth. Design and pitch new products, services, and other initiatives to a leadership team consisting of serial entrepreneurs and seasoned executives and backed by a board of directors consisting of industry veterans of energy, finance, and government.

Hut 8

Head of Regulatory and Government Affairs

ea_via_bold

Assess 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.

Openwork

Manager, Regulatory Affairs

dstribute

Join Our Team: Where We Belong Position Overview The Assistant Program Director of Clinical Affairs (APD-CA) of the Master of Health Science in Anesthesia (MHSA) program at Burrell College of Health Sciences is responsible for overseeing, coordinating, and quality-managing clinical practicum experiences that form the backbone of the MHSA curriculum. Didactic learning continues throughout the full curricular continuum, transitioning from in-person to virtual delivery during clinical rotations, and the APD-CA coordinates with academic leadership to ensure that the clinical experience remains coherent with and reinforced by concurrent didactic content.

Burrell College of Health Sciences

AA - Assistant Program Director of Clinical Affairs - (MHSA)

ADMA Biologics Inc

Department: Influence I Government Affairs Reports To: Chief Operations Officer FLSA Classification: Salary | Exempt Supervision: None Work Schedule: M–F | 8:00am – 4:30pm | Occasional evenings and weekends for events and advocacy activities Travel: Occasional local and state travel may arise for government meetings, coalition events, advocacy activities, and community forums Position Overview The Director of Government Affairs serves as the primary point of contact between ORRA, its members, elected officials, and external political and community organizations. CORE COMPETENCIES Competency What It Looks Like in This Role Advocacy & Policy Expertise Demonstrates a working command of legislative processes, public policy development, and regulatory tracking; translates complex issues into clear, actionable strategies that advance ORRA’s positions and protect member interests.

Association

Director of Government Affairs

sourcestack_via_bold

Authors US FDA premarket submission (e.g., 510(k), Q-submissions) and international submissions for medical devices, including software devices (SaMD, SiMD), with collaboration from key staff in Product Development, Operations, Marketing, and Quality for timely submissions. Minimum of nine (9) years of Regulatory Affairs related experience in a medically regulated environment with at least seven (7) years in a medical device company (US FDA Class II) and two (2) years software medical device (SaMD, SiMD) experience is required.

Treace Medical Concepts Inc

Principal Regulatory Affairs Specialist - Software Devices

linkup_via_bold

Work Location: This position is fully remote and open to candidates residing in the U.S., excluding Alaska; Delaware; Hawaii; Louisiana; Montana; North Dakota; Oklahoma; West Virginia; Wyoming; and U.S. Territories. The Medical Director Scientific Affairs provides strategic leadership to the Clinical Policy team, ensuring medical and pharmacy policies are rigorously evidence-based and aligned with current clinical advancements.

Oscar Health

Medical Director Scientific Affairs

GreenHouseAPI

Furthermore, the Assistant Dean will lead, train and mentor faculty and staff to achieve the strategic vision and mission of the Office of Undergraduate Affairs and ensure compliance with applicable internal/external regulations and ensure that program outcomes are consistent with the University's goals and objectives. The Director, Undergraduate Affairs Administration will be responsible for assisting the Dean of Undergraduate Affairs in day-to-day and strategic activities and oversight to the undergraduate programs within the Office of Undergraduate Affairs.

University of Miami

Director, Undergraduate Affairs Administration

For California Residents: We may collect the following categories of personal information in connection with the submission of your resume or application materials to us for employment, and if hired, your employment with us: identifiers (e.g., name, address, email address, birthdate); personal records (e.g., telephone number, signature, education information, criminal background information, passport number and visa information); consumer characteristics (e.g., sex, marital status, veteran status, race, disability, sexual orientation); professional or employment information (e.g., resume, cover letter, employment history, background check forms, references, certifications, transcripts and languages spoken); and inferences from personal information collected (e.g., a profile reflecting abilities and aptitudes). The above categories of personal information are collected for the following business purposes: performing recruitment and hiring services; processing interactions and transactions (e.g., to comply with federal and state laws requiring us to maintain certain records, managing the workforce); and security (e.g., detecting security incidents, protecting against fraudulent or illegal activity).

Dentsply Sirona Inc

Regulatory Affairs Manager, OAS

The 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.

Aso LLC

Regulatory Affairs Manager

Dentsply

FULL_TIME

Lennar Homes

You will act as the Latin America regulatory subject matter expert and internal point of contact, maintaining alignment with key stakeholders across the company, and ensuring regulatory priorities in the region support the company’s commercial goals. You will guide Dexcom’s regulatory staffing strategy for Latin America: attracting talent, developing new team members, and strengthening Dexcom’s regulatory capability in the region.

DexCom

Sr Manager Regulatory Affairs- LATAM

Partnering cross-functionally across Quality, Network Management, and Compliance, this leader optimizes provider onboarding to deliver a high-quality, compliant network that supports member access and organizational growth. Serve as a subject matter expert on state and federal healthcare regulations, continuously monitoring legal developments and translating regulatory changes into proactive operational updates to maintain ongoing compliance.

Associate Medical Director, Regulatory Management

You'll help ensure that board and committee activities, corporate records, regulatory requirements, and legal processes are executed efficiently and accurately, while also supporting broader legal initiatives that contribute to the organization's growth, compliance, and long-term success. Demonstrated ability to independently manage recurring board and committee governance processes, anticipate governance requirements and deadlines, and appropriately escalate legal, regulatory or governance matters, with appropriate Legal oversight.

Itau

Sr Corporate Governance and Legal Affairs Specialist

Together, you'll explore new ideas, challenge assumptions, and shape solutions that make a real-world impact by: Lead teams and cross-functional partnerships with surgeons and operating room stakeholders to accelerate adoption of Restrata and related products through clinical education, customer engagement, and operational excellence. Through Acera Surgical and the Restrata product, the team advances evidence‑based wound care technologies that support healing across multiple surgical specialties, helping frontline healthcare providers deliver safer, more effective care.

Director Of Regulatory Affairs Jobs in Florida

Sr. Director; Regulatory Affairs Visa

Director, Thought Leader Engagement (H&N) - Southeast Genmab

Chief Compliance Officer Lennar Corporation

Senior Director, Regulatory Affairs (Inhalations – ANDAs and 505 (b)(2)) Lupin Pharmaceuticals Inc.

Head of Regulatory and Government Affairs Hut 8

Manager, Regulatory Affairs Openwork

AA - Assistant Program Director of Clinical Affairs - (MHSA) Burrell College of Health Sciences

Manager, Regulatory Affairs ADMA Biologics Inc

Director of Government Affairs Association

Principal Regulatory Affairs Specialist - Software Devices Treace Medical Concepts Inc

Medical Director Scientific Affairs Oscar Health

Director, Undergraduate Affairs Administration University of Miami

Regulatory Affairs Manager, OAS Dentsply Sirona Inc

Regulatory Affairs Manager Aso LLC

Regulatory Affairs Manager, OAS Dentsply

Chief Compliance Officer Lennar Homes

Sr Manager Regulatory Affairs- LATAM DexCom

Associate Medical Director, Regulatory Management Oscar Health

Sr Corporate Governance and Legal Affairs Specialist Itau

Acera Area Sales Director - West FL/AL (West Coast of Florida including Orlando and the Panhandle and Alabama) Solventum Corp

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