FULL_TIME

FEED

UNKNOWN

Regulatory strategy: Develop, own and execute Xcimer’s licensing and permitting strategy for current and future facilities, including pathway selection across the U.S. Nuclear Regulatory Commission (NRC) byproduct-material framework and Agreement State programs, jointly with Engineering leadership. Site and environmental permitting: Lead non-technical environmental review and site permitting activities, including National Environmental Policy Act (NEPA) processes where federal funding or action applies, and air, water, land-use, and zoning approvals, working with Capital Projects/Facilities and outside consultants.

Xcimer Energy

Director, Licensing & Regulatory Affairs

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Reporting to the SRA Director for Accelerator leading the Better For You (BFY) SRA team for the Accelerator business-the division supporting KIND, Tru Fru, Nature's Bakery, and the newly acquired Kellanova brands. The SRA Specialist works cross-functionally with project teams to proactively identify potential regulatory problems, provide guidance and assist in creating a positive compliance environment for our products and business goals.

Mars Inc

Scientific and Regulatory Affairs Specialist

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Committee and Member Office Relationships: Build and maintain relationships with professional staff on the House and Senate Appropriations Subcommittees on Defense (HAC-D, SAC-D) and the House and Senate Armed Services Committees (HASC, SASC), including relevant subcommittees with jurisdiction over tactical air and land forces, intelligence and special operations, and emerging threats. In concert with the VP of Washington Operations, the Director serves as the company''s primary interface with professional staff on the defense subcommittees and personal office staff, translating Sentinel''s counter-UAS, autonomous systems, and stratospheric ISR portfolio into actionable legislative outcomes - funding lines, authorization language, and report direction that advance company programs.

YEAR

DZYNE Technologies

Director of Government Affairs

The Director, Regulatory Affairs -Biologics is responsible for executing the global regulatory strategy and for the company's biologics portfolio across the full product lifecycle, from early development through regulatory approval, commercialization, and post-approval lifecycle management. The successful candidate will bring experience with biologics development, global regulatory requirements, commercial manufacturing, and lifecycle management, combined with strong leadership skills and the ability to operate effectively in a dynamic biotechnology environment.

Vericel Corp

Director, Regulatory Affairs - Biologics

Reporting directly to the Chief Medical Officer, you will develop and implement global regulatory strategies supporting multiple therapeutics - small molecules, biologics, and oligonucleotides - and diagnostics across our three therapeutic areas: neurology/neurodegeneration, metabolism/cardiovascular, and ophthalmology. You will be at the forefront of implementing and influencing new regulatory policy across multiple jurisdictions using objective, data-driven approaches, treating health authorities as key partners who share our vision of bringing better, more targeted drugs to patients faster.

Insitro Inc

Vice President, Regulatory Affairs

Chemistry, Communication, Continual Improvement Process, Data Compilation, Environmental Science, Food Safety and Sanitation (Inactive), Food Sciences, Food Technology, Green Solutions, Laboratory Testing, Leadership, Microbiological Test, Product Development, Quality Control (QC), Researching, Sensory Testing, Sustainability, Waterfall Model Pay Range: In this highly visible Scientific & Regulatory Affairs (SRA) – Nutrition role, you will help translate nutrition science, regulatory developments, consumer insights, and emerging health trends into actionable business strategies that protect the enterprise and fuel business growth for The Coca-Cola Company North America.

Corinth Coca-Cola currently operates in Corinth, Miss.; Tupelo, Miss; Lexington, Tenn.; and Jackson, Tenn. 
Upon the completion of its territory expansion, Corinth Coca-Cola will operate in five states and increase its headcount
by almost 30% to approximately 450 associates.

Corinth Coca-Cola Bottling Works, Inc. is a privately held, family-owned Coca-Cola bottling and distribution
company. Founded by Avon Kenneth Weaver and C.C. Clark in 1907 in Corinth, Miss., Weaver descendants
continue to own and operate the company today. In addition to its headquarters in Corinth, Corinth Coca-Cola
Bottling Works currently has locations in Lexington, Tenn.; Jackson, Tenn.; and Tupelo, Miss. 

For more information, visit www.corinthcoke.com.


Coca-Cola

Director, Scientific & Regulatory Affairs - Nutrition

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Serves as a therapeutic area thought leader and interacts with experts in the field to obtain feedback on clinical aspects of US and global products and new data generation, interpretation and dissemination. Minimum $230,720.00 - Maximum $345,000.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States.

Otsuka

Senior Director Global Medical Affairs Inborn Errors of Metabolism

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This role is responsible for developing and executing state and local legislative strategies to advance AHLA's policy priorities, including proactive and defensive advocacy campaigns, coalition engagement, and stakeholder mobilization. The American Hotel & Lodging Association (AHLA) is seeking a Director of State & Local Affairs to develop and execute government affairs and public policy strategies in various markets throughout the United States.

AHLA

Director Of State And Local Affairs

As a Senior Regulatory Affairs Specialist, you will be a hands-on regulatory partner across our product and research teams: setting regulatory paths at the requirements stage, reviewing what our products say and do, supporting FDA and international submissions, and keeping regulatory records audit-ready. Through comprehensive lab testing, MRI and CT imaging, longitudinal data, and guidance from AI and clinical teams, Function gives members a complete and continuous view of their health, and the clarity to act on it.

Function Health

Senior Regulatory Affairs Specialist

ADAPTED_NOW

Responsibilities : Commercial Regulatory Affairs (CORA) is part that interprets the needs of worldwide health authorities and provides regulatory intelligence necessary to generate and present information that meets the needs of health authorities, patients, purchasers and prescribers for the firm's global Pharma Division, which includes all therapeutic areas and all phases of product development from early development to post marketing. Must demonstrate in-depth knowledge of the bio/pharma industry (compliance, legal, clinical affairs, regulatory and product marketing) as well as in-depth knowledge of the legal and regulatory environment, as it relates to healthcare compliance in the bio/pharma industry (includes anti-kickback statutes, government fraud & abuse, off-label promotion, PhRMA Code, etc.).

SGA Inc.

Senior Program Director, Commercial Regulatory Affairs

SGA Inc

In conjunction with regulatory affairs leadership, he/she will develop strong relationships, collaborate, and interact with various departments and levels of management, including interactions across BridgeBio subsidiaries. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process.

BridgeBio Pharma Inc

Associate Director, Regulatory Affairs - CMC

In consultation and coordination with a cross-functional team across the company's policy, legal and business organizations, the position coordinates and supports litigation positions, builds external coalitions, engages with external stakeholders, and supports advocacy strategies to realize regulatory outcomes that create value for the company. Manage the company's regulatory affairs activity in contested cases and similar proceedings before state utility commissions, including support for and development of litigation positions, building external coalitions, and executing regulatory affairs strategies to realize outcomes that create value for the company.

Constellation Energy Generation, LLC.

Manager - Regulatory Affairs

[AW]-iCims

In a normal week we are negotiating power offtake agreements, closing supply and equipment contracts for major assets, working offshore lease applications, standing up project companies around the world, and supporting a venture-backed hardware startup. By leveraging modular design, manufacturing scale, efficient drilling, and latent cooling on the seafloor, we are pioneering a new category of energy that outperforms traditional sources on environmental impact, deployment speed, and cost.

Endurance Energy

Director of Legal Affairs

Your primary focus will be federal affairs, building and sustaining relationships across the House and Senate while partnering with government affairs teams at health systems, hospital associations, and other key healthcare stakeholders to drive aligned, high-impact initiatives. Madison, a city surrounded by water, has received accolades for being the greenest city in America (NerdWallet), the best city for renters (SmartAsset), the fittest city in America (Fitbit), and the third best metro in the US for young professionals (Forbes Advisor).

Epic Systems Corp

Director of Federal Government Affairs

Ensure that associates are accountable for timely development of clinical trial documentation including instructions for use, case report forms (CRFs), CRF guidelines, informed consent, monitoring plans and reports, assisting with study protocol development and other necessary clinical/regulatory documentation. This position will be responsible for understanding the operating principles of the devices required, to develop preclinical and clinical evaluation plans including study protocols; determine study documentation requirements; and generate final reports and sections of FDA applications.

Sysmex America Inc

Director, Clinical Affairs

Develops and leads execution of AV's congressional advocacy and engagement strategies; manages consultant lobbyist relationships and resources, and fully complies with lobby laws, lobby disclosure and assists with Political Action Committee management (filing PAC reports and statements, depositing & dispersing funds, authorizing expenditures, advocating for contributions). Coordinates and supports AV U.S. Government customer interaction in Washington D.C. Develops and maintains relationships with Members of Congress, congressional committees and personal staff members; identifies and coordinates opportunities for AV leadership interaction with Congress.

Who We Are
Based in California, AeroVironment (AVAV) is a global leader in unmanned aircraft systems (UAS) and tactical missile systems. Founded in 1971 by celebrated physicist and engineer, Dr. Paul MacCready, we&rsquo;ve been at the leading edge of technical innovation for more than 45 years. Be a part of the team that developed the world&rsquo;s most widely used military drones and created the first submarine-launched reconnaissance drone, and has seven innovative vehicles that are part of the Smithsonian Institution&rsquo;s permanent collection in Washington, DC.
Join us today in developing the next generation of small UAS and tactical missile systems that will deliver more actionable intelligence to our customers so they can proceed with certainty &ndash; and succeed.
We offer our employees&nbsp;full medical, dental, vision benefits all&nbsp;beginning&nbsp;day 1 of employment.&nbsp; &nbsp;For more details visit: <a href="http://www.myavbenefits.com">www.myavbenefits.com</a> Paid time&nbsp;off:&nbsp;&nbsp;2 weeks vacation, plus paid company holiday shut down Dec. 25 - Jan 1. 9/80 work schedule: every other Friday off! A fun and collaborative work environment encouraging personal growth and creative innovation;&nbsp;AV is a tech start-up with stability.

Aerovironment

Legislative Affairs Director

As a member of the leadership team, you will partner closely with the CEO and leaders across R&D, Engineering, Clinical Affairs, Operations, and Commercial to assess current capabilities, establish clear priorities, and build the people, processes, and systems required to advance clinical milestones and support long-term commercialization. Align clinical evidence with the path to approval by partnering with Clinical Affairs, scientific advisors, and clinical investigators to ensure study designs, endpoints, and evidence support regulatory submissions, product development, and commercialization.

Blackrock Neurotech LLC

VP, Regulatory Affairs & Quality Assurance

Proven leadership in compliance with an ability to troubleshoot within FDA and international regulations and guidelines including, but not limited to, clinical strategy, GCPs, GLPs, SOPs, submissions, product launch, labeling, advertising and promotion, product vigilance, and medical device reporting. He or she should know regulatory road maps for medical devices and preferably combination drug-device products, which will speed up the clinical trial cycle, the regulatory process and garner more government resources.

Sight Sciences Inc

Primary coverage includes active participation in ERCOT and SPP stakeholder processes and related proceedings, with additional engagement across states where Scout operates and develops projects (currently including Texas, South Dakota, Oklahoma, Missouri, and North Dakota; coverage may evolve). Because Scout's portfolio in this region is weighted toward operating projects, the role will focus on issues that affect day-to-day operations and commercial outcomes and will help craft and advocate for rules that are stable, effective, and aligned with renewable resources' technical capabilities.

Scout Clean Energy

Manager, Government And Regulatory Affairs - SPP And Ercot

Primary coverage includes active participation in ERCOT and SPP stakeholder processes and related proceedings, with additional engagement across states where Scout operates and develops projects (currently including Texas, South Dakota, Oklahoma, Missouri, and North Dakota; coverage may evolve). Because Scout’s portfolio in this region is weighted toward operating projects, the role will focus on issues that affect day-to-day operations and commercial outcomes and will help craft and advocate for rules that are stable, effective, and aligned with renewable resources’ technical capabilities.

Director Of Regulatory Affairs Jobs in the United States

Director, Licensing & Regulatory Affairs Xcimer Energy

Scientific and Regulatory Affairs Specialist Mars Inc

Director of Government Affairs DZYNE Technologies

Director, Regulatory Affairs - Biologics Vericel Corp

Vice President, Regulatory Affairs Insitro Inc

Director, Scientific & Regulatory Affairs - Nutrition Coca-Cola

Senior Director Global Medical Affairs Inborn Errors of Metabolism Otsuka

Director Of State And Local Affairs AHLA

Senior Regulatory Affairs Specialist Function Health

Senior Program Director, Commercial Regulatory Affairs SGA Inc.

Associate Director, Regulatory Affairs - CMC BridgeBio Pharma Inc

Manager - Regulatory Affairs Constellation Energy Generation, LLC.

Director of Legal Affairs Endurance Energy

Director of Federal Government Affairs Epic Systems Corp

Director, Clinical Affairs Sysmex America Inc

Legislative Affairs Director Aerovironment

VP, Regulatory Affairs & Quality Assurance Blackrock Neurotech LLC

Vice President, Regulatory Affairs Sight Sciences Inc

Manager, Government And Regulatory Affairs - SPP And Ercot Scout Clean Energy

Manager, Government and Regulatory Affairs - SPP and ERCOT Scout Clean Energy

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