1,162 Results for

Regulatory Affairs Manager Jobs in Washington, DC

Jobs

Sriracha, CHO30+ days ago

li>Ensure LRN is updated with new employee information for new hires, delete terminated employees, make sure all employees are compliant with training requirements by due date and train employees in a classroom setting for those that do not have email addresses.

Full spectrum of Payroll management function such as collect & checking data, payroll processing, payment and summary report (Month-End, Year-End, Tax, Social Security Fund, etc.).

New!

Gaithersburg, MD6 days ago

$109,245–$163,867 Per Year

li>Integrated Project Management: Develop, execute and maintain submission delivery plans and content plans; proactively provide status updates to stakeholders; coordinate input, maintenance and revisions in Planit project plans; highlight unforeseen changes in resource demand to the Lead RPM and line manager.

Submission Leadership: Lead and contribute to planning, preparation (including authoring where relevant) and delivery of simple and, with experience, increasingly complex submissions throughout the product lifecycle from global and/or regional perspectives; connect immediate deliverables to future label and lifecycle opportunities.

Baltimore, MD30+ days ago

li> Provide leadership to Subject Matter Experts (SMEs) in multidisciplinary teams and manage day to-day operations of project tasks/activities to ensure deliverables are met in a timely manner within budget.

Experience with multiple electronic software/platforms (such as Vantagepoint, Starting Point templates (or similar regulatory templates), Smartsheet, MS Office suite or other project management programs).

Washington, District of Columbia30+ days ago

p style="min-height:1.5em">Learn more about our vision, team, and backers athttps://www.emeraldai.co/.

Preferred style="min-height:1.5em">Experience working with or before state Public Utility Commissions and/or the Federal Energy Regulatory Commission (FERC).

DC12 days ago
p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html.
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position.

Rockville, MD30+ days ago
$100,000–$140,000 Per Year
p>Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. The worker is required to have close visual acuity to perform an activity such as preparing and analyzing data and figures; transcribing; viewing a computer screen, iPad, or other electronic device; and extensive reading.

Germantown, MD27 days ago
li>Participation in project team and sub team discussions regarding preclinical, clinical and CMC aspects of drug development, providing regulatory guidance, communicating regulatory goals and timelines, and helping to ensure compliance to the requirements from U.S. and foreign regulatory agencies.
The Associate Director/Senior Manager will interact with all aspects of Precigen's quality, CMC, preclinical, and clinical drug development programs, policies, and procedures ensuring compliance is maintained with all regulatory commitments/requirements.

DC30 days ago
Remote
While most day-to-day interactions will be conducted virtually, this position requires a proactive communicator who can effectively engage in a hybrid environment, balance independent remote work and occasional on-site presence with internal and external stakeholders to support team alignment and relationship-building. Job Summary: Lead the RAC-Safety team to ensure that all safety regulatory, certification and compliance matters affecting current and future vehicle content/design/development/performance are fully supported, and that items of importance to Mitsubishi Motors are reported on in a timely manner.

Arlington, VA30+ days ago
ul>
Drafting and refining regulatory response letters - working with sites to compose accurate, legally compliant responses to government agencies (particularly OSHA Complaint Response Letters and similar regulatory inquiries).
Quality control and documentation - reviewing response letters for spelling, grammar, tone, and clarity before submission;
Managing regulatory documentation - handling attachments and ensuring sensitive information is properly redacted.

Rockville, MD19 days ago
$113,850–$189,750 Per Year
GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. Site Name: USA - Maryland - Rockville, Hamilton Montana, USA - Pennsylvania - Upper Providence Posted Date: Jun 9 2026 At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade.

Arlington, VA30+ days ago
p>Amazon is seeking an experienced Workplace Health & Safety (WHS) professional to join the Governance Regulatory Response and Activity (RRA) team who will be responsible for regulatory response case managing. This role combines strategic planning with practical implementation to ensure regulatory compliance and promote a safety-first culture of all Amazon operations in North America.

DC23 days ago
You will also partner with teams across Google and Alphabet's Public Policy, Compliance, Legal, Engineering, Finance and product areas to support the handling of some of the most important issues for the company today.
In this role, you will work closely with members of Regulatory Affairs and act as the central operations support for the department"s role in the broader regulatory lifecycle.

District of Columbia30+ days ago
Reporting to the Head of Government Affairs, this individual will play a critical role in advancing Broadridge's policy priorities by building and maintaining relationships with key federal officials, monitoring legislative and regulatory developments, and positioning Broadridge as a trusted resource among policymakers and industry stakeholders.
The ideal candidate brings deep knowledge of the financial services regulatory landscape, a strong network on Capitol Hill and within federal agencies, and the ability to translate complex regulatory issues into clear, compelling narratives for a variety of audiences.

District of Columbia30+ days ago
p style="text-align:inherit"/>
This position is responsible for leading and supervising the Company’s Government, Regulatory and Public Affairs team; identifying, interpreting and responding to legislative and regulatory activity that may impact the company; designing and implementing advocacy strategies to advance the Company’s policy priorities; acting as the company’s chief federal lobbyist and overseeing lobbying and advocacy activities in key states; managing and overseeing the company’s engagement with trade associations, coalitions and third party advocacy organizations and developing and implementing the company’s political engagement strategy.
Develop and maintain relationships with public policy organizations influential within the areas of home-based and personal care, Medicaid and other federal healthcare programs as well as organizations focused on access to care, transportation policy, and community-based health services, including PCS/ HCBS provider and consumer advocacy stakeholders.

DC30+ days ago
$202,300–$283,200 Per Year
p>This position is responsible for leading and supervising the Company's Government, Regulatory and Public Affairs team; identifying, interpreting and responding to legislative and regulatory activity that may impact the company; designing and implementing advocacy strategies to advance the Company's policy priorities; acting as the company's chief federal lobbyist and overseeing lobbying and advocacy activities in key states; managing and overseeing the company's engagement with trade associations, coalitions and third party advocacy organizations and developing and implementing the company's political engagement strategy.
Develop and maintain relationships with public policy organizations influential within the areas of home-based and personal care, Medicaid and other federal healthcare programs as well as organizations focused on access to care, transportation policy, and community-based health services, including PCS/ HCBS provider and consumer advocacy stakeholders.

DC30+ days ago
$180,000–$190,000 Per Year
Reporting to the Head of Government Affairs, this individual will play a critical role in advancing Broadridge's policy priorities by building and maintaining relationships with key federal officials, monitoring legislative and regulatory developments, and positioning Broadridge as a trusted resource among policymakers and industry stakeholders.
The ideal candidate brings deep knowledge of the financial services regulatory landscape, a strong network on Capitol Hill and within federal agencies, and the ability to translate complex regulatory issues into clear, compelling narratives for a variety of audiences.

New!
Washington, DC3 days ago
Congress), or responses to legislative inquiries; strong legal research skills and the ability to interpret complex statutes and regulations, particularly those applicable to commercial motor vehicle safety, (which may include medical, health, and physical qualifications, drug and alcohol testing programs, electronic data systems, or emerging technologies like automation or cyber-security, among others); an extensive working knowledge of the Administrative Procedure Act, statutes related to regulatory evaluation, and executive orders and procedures applicable to the Federal rulemaking process; strong communication skills both orally and in writing (drafting and editing); and the ability to work effectively in a collaborative team environment, as well as the ability to work independently with limited direct supervision.
The Attorney-Advisor in the Regulatory and Legislative Affairs division of the Federal Motor Carrier Safety Administration serves as the legal counsel to agency regulatory development teams and provides legal advice, document drafting, and legal sufficiency review of regulatory instruments including rulemaking notices involving motor carrier and driver safety; hazardous material transportation; and motor carrier licensing, operations, and commercial regulations.

Arlington, VA30+ days ago
By supporting our customer teams at fulfillment centers and AIR sites to implement process improvements, mitigate risk, resolve equipment issues, and implement new processes to improve performance, AvSec contributes to safe and secure transportation of air cargo to our customers. As part of Amazon's global aviation security team, you will support Amazon Air, Prime Air, Amazon Global Logistics, and Amazon's broader aviation operation by transforming traditional compliance approaches and establishing Amazon as a thought leader in aviation security regulation.

New!
Washington, DC3 days ago
The Regulatory Affairs Coordinator will support the center's human subjects research portfolio focused on environmental exposures and health outcomes, by preparing, submitting, and managing regulatory documentation; ensuring compliance with institutional, federal, and sponsor requirements; and assisting with study budget and supply management. This role is responsible for Institution Review Board (IRB) submissions, informed consent oversight, regulatory documentation management, supply tracking, ongoing study compliance, supply inventory, and study budget oversight.

Gaithersburg, MD30+ days ago
$157,500–$262,500 Per Year
p>Experience & knowledge Essential:
• Solid track record in drug development and leadership within a dynamic project team • Emerging understanding of global regulatory requirements to be able to formulate tactical regulatory strategies • Ability to prepare and submit regulatory documentation to ensure regulatory compliance globally • Emerging ability to propose scientific regulatory strategies that are reviewed with line management for concurrence and approval • Excellent knowledge of US regulatory requirements and experience with submissions gained within drug development.
The individual will also be assigned projects and regulatory activities by providing expertise to Immunocores development programs to include regulatory implementation of regulatory strategies, IND developments, submission, maintenance, tracking BLAs, BLA planning, submission, maintenance, tracking agency liaison for specific tactical assignments and regulatory intelligence for tactical process-related changes in requirements.

Germantown, MD30+ days ago
Create practical solutions to complex regulatory challenges by setting policies and procedures, aligning cross-functional teams, and maintaining strong working relationships with government and non-government organizations that affect market access and distribution.
Strategic experience and ability, having demonstrated success related to the development and implementation of pre-clinical and clinical strategies for clinical IVD products, implementation of regulatory systems, and assuring compliance to all applicable regulations.

Arlington, VA30+ days ago
p>Qualifications:
• 10+ years in satellite policy, regulatory affairs, or telecom law within the satellite or aerospace sector • Strong network of relationships across government agencies, space industry bodies, and regulatory institutions • Deep knowledge of FCC and ITU frameworks and procedures • Knowledge of orbital debris mitigation policy and space sustainability frameworks • Strong experience reporting to executive teams and boards, including preparation of regulatory or strategy briefings • Demonstrated success leading teams and working cross-functionally • Track record of representing organizations at high-level international policy forums (e.g., WRC, UN COPUOS) • Willingness to travel approximately 25% of the time.
Preferred Skills & Experience:
• Leadership experience with global satellite operators, launch providers, or legal/regulatory advisory firms • MBA, MSEE, JD, or equivalent advanced degree in a related field • Technical expertise in RF engineering, satellite systems, and/or inter-satellite links • Experience with spectrum requirements for commercial space launch, lunar operations • Background in national security space policy and ITAR/EAR compliance • Proven ability to navigate complex multi-stakeholder regulatory challenges • Experience leading through organizational growth and transformation.

Gaithersburg, MD27 days ago
$295,600–$347,764 Per Year
p>Your Role:
The role will be responsible to lead the regulatory strategy for US Biomedicine efforts in alignment with global efforts.?The role will oversee industry-specific practices, ensure all government and company regulations are being met, assessing regulatory risks and interfacing with regulatory authorities to ensure the company meets all set requirements and guidance's.
Lead team members that provide regulatory affairs content and requirements for regulatory submissions and review this content for conformance with established requirement.?Manage and develop staff, if required, including staff professional development and project oversight accountability.?.

McLean, Virginia27 days ago
GEA teams include Regulatory Affairs, Risk, Innovation, Strategy and Enablement (RISE), Community Impact and Investment (CII), Community Finance, CRA Strategy and Program Management, Global Policy Affairs Group (GPAG), and Global Enterprise Communications (GEC).
Own timely execution of monthly and quarterly horizontal reporting deliverables related to strategic and operational priorities, and partner with leadership to shape, align, and execute strategic priorities across teams and towers to help ensure that programs related are well managed.

Gaithersburg, MD30+ days ago
$178,534–$267,801 Per Year
p>Competitive salary and benefits package on offer:
Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles) or to receive a retirement contribution (hourly roles).

Rockville, MD7 days ago
$113,850–$189,750 Per Year
GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment.

Gaithersburg, MD10 days ago
$218,058–$327,087 Per Year
p>Accountabilities:
Global Regulatory Leadership: Own the end-to-end global regulatory strategy for a high-complexity cell and gene therapy program, from current stage through BLA submission, ensuring an efficient route to approval with competitive labeling aligned to product attributes and patient, market and business needs.
Cross-Functional Product Leadership: Represent Regulatory Affairs on Global Product Teams, shaping development and commercialization plans, contributing to governance presentations and aligning regulatory objectives with clinical, CMC, safety and commercial strategies.

New!
Gaithersburg, MD3 days ago
p>Accountabilities:
Global Regulatory Leadership: Own the end-to-end global regulatory strategy for a high-complexity cell and gene therapy program, from current stage through BLA submission, ensuring an efficient route to approval with competitive labeling aligned to product attributes and patient, market and business needs.
Cross-Functional Product Leadership: Represent Regulatory Affairs on Global Product Teams, shaping development and commercialization plans, contributing to governance presentations and aligning regulatory objectives with clinical, CMC, safety and commercial strategies.

Washington, District of Columbia19 days ago
The primary roles and responsibilities include managing the development of regulatory submissions, development of overall regulatory strategy, communicating with regulatory bodies and clients, and leading or expanding new therapy ideas, as applicable.
Develop and execute regulatory services for client companies, including however not limited to:
Regulatory Submissions (e.g., 510(k), IDE, PMA, IND, BLA, & IND, Technical Documentation, STED, CERs).

Washington D. C., Washington, DC21 days ago
$79,000–$124,000 Per Year
What you'll need:
5+ years of experience supporting senior executives in a fast-paced corporate environment, preferably in government affairs, regulatory, legal, technology, aerospace, telecommunications, or similarly complex global environments.
Team Integration:
Facilitating collaboration within the Global Government Affairs & Regulatory team, managing logistics for team meetings, offsites, and special projects to drive organizational efficiency.

Gaithersburg, MD25 days ago
$135,624.80–$203,437.20 Per Year
p>The Associate Regulatory Affairs Director, US Lead, Regulatory Science & Execution will be accountable for the development, implementation and maintenance of regulatory strategies for assigned project(s)/product(s) and regulatory jurisdiction(s), with the intention of achieving successful registration and lifecycle management of unique and technologically complex products serving patients with rare diseases and unmet medical needs.
Providing strategic and tactical advice on regulatory issues for pipeline products; actively collaborates with management, Global Regulatory Lead, and cross functional colleagues within Alexion (i.e., commercial, research, clinical development, medical affairs, business development, legal, manufacturing, quality, portfolio management, financial, human resources, etc.).

Washington, WA30+ days ago
$248,000–$310,000 Per Year
Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. This role combines senior‑level regulatory policy leadership, regulatory intelligence, and external advocacy, with accountability for shaping US regulatory outcomes, enabling development and portfolio strategy, and strengthening Teva's influence and credibility with FDA and key stakeholders.

DC30+ days ago
Our history spans over 200 years and today we are a leader in investment banking, consumer and small business banking, commercial banking, financial transaction processing and asset management.
JPMorgan Chase, one of the oldest financial institutions, offers innovative financial solutions to millions of consumers, small businesses and many of the world's most prominent corporate, institutional and government clients under the J.P.

Germantown, MD27 days ago
p>This role is responsible for defining regulatory strategy, planning and the preparation of US and eventually global regulatory submissions to achieve timely approvals of biologic licensing and marketing authorization applications and post-approval lifecycle changes for Precigen CAR-T and AdenoVerse immunotherapy Products.
We are seeking a global Executive Director, Regulatory Affairs (level determined by candidate experience) reporting into the SVP Regulatory Affairs who is responsible for oversight of IND/IMPD, BLA and ex-US activities for the CAR-T and immunotherapy products.

MD30+ days ago
$220,000–$230,000 Per Year
p>As a Government Affairs Director, Spectrum Policy & Regulatory Affairs you will be responsible for:
Developing and implementing spectrum policy and regulatory positions in support of MSI business goals and objectives, coordinating MSI spectrum and regulatory strategies between different regulatory regimes, balancing the differences in spectrum availability and regulations between countries to advance MSI interests.
Represent MSI externally at regional and international spectrum conferences such as the World Radio Conference, and at industry, public safety and other trade association conferences and meetings (e.g., TIA, EWA, IWCE, APCO) acting as the face of MSI on such issues.

DC30+ days ago
In doing so, you will partner with product, legal, communications, government affairs, and trust and safety teams across the company to develop and execute our policy strategy, analyze and respond to new legislative and regulatory proposals, and craft our external narrative on key policy issues. 7 years of experience working on technology or content policy issues within industry, government, think tanks, public interest groups, or industry associations on issues related to copyright, intellectual property, and media/publisher policy issues.

Gaithersburg, MD17 days ago
$135,624.80–$203,437.20 Per Year
p>The Associate Regulatory Affairs Director, US Lead, Regulatory Science & Execution will be accountable for the development, implementation and maintenance of regulatory strategies for assigned project(s)/product(s) and regulatory jurisdiction(s), with the intention of achieving successful registration and lifecycle management of unique and technologically complex products serving patients with rare diseases and unmet medical needs.
Providing strategic and tactical advice on regulatory issues for pipeline products; actively collaborates with management, Global Regulatory Lead, and cross functional colleagues within Alexion (i.e., commercial, research, clinical development, medical affairs, business development, legal, manufacturing, quality, portfolio management, financial, human resources, etc.).

Washington, Washington, DC30+ days ago
The position is involved in all aspects of the federal affairs department, including lobbying strategy and execution (using both internal and external resources), developing and maintaining relationships with external stakeholders across the political spectrum, drafting policy briefings and memorandum, tracking federal legislation, trade association participation, and leveraging Executive participation with federal officials. In addition, for certain issues as assigned by the Vice President, Government Affairs, this position serves as an issue manager responsible for leading, coordinating and integrating all public affairs initiatives, programs, communications and activities with key stakeholders to support the strategic needs of the business.

DC16 days ago
Working closely with Google leaders, GAPP seeks to identify key policy issues, listen carefully to others' views and opinions, and distill and share the company's perspective on those issues with external stakeholders. You will join the Global Policy Campaign team within the GAPP Centers of Excellence, working across geographies and functions to drive campaigns that support key policy priorities.

Gaithersburg, MD10 days ago
$186,232–$279,349 Per Year
Partnering with senior leaders and global teams, you will lead strategy across key milestones-from expedited designations and Health Authority interactions through major submissions and post-approval maintenance-helping the business deliver transformative therapies at pace and with rigor.
In this Director role, you will shape the regulatory path for programs that span oncology, immune-mediated and rare diseases-translating breakthrough science into timely approvals and competitive labeling that make a tangible difference to patients and markets.

DC27 days ago
From software to hardware our teams are shaping the future of world-leading hyperscale computing, with key teams working on the development of our TPUs, Vertex AI for Google Cloud, Google Global Networking, Data Center operations, systems research, and much more. Operational Frameworks and Workflow Optimization: Establish centralized processes and frameworks to align disparate team priorities, monitor project milestones, anticipate bottlenecks, and streamline workflows across multiple states.

DC24 days ago
$120,800–$151,000 Per Year
This role helps advance company policy priorities in key states by executing legislative and regulatory strategies, maintaining relationships with policymakers and stakeholders, and partnering cross‑functionally to mitigate risk and support business objectives.
Serve as a state lobbyist in priority states, including drafting and negotiating bill language, supporting sponsor engagement, delivering or coordinating testimony, and assisting with committee and floor strategy.

DC30+ days ago
p>Drive end-to-end federal/state/local public affairs activities related to the GBSG and CR portfolio, including strategic alliances, third-party outreach, and amplification of the company's messaging to help shape specific legislative, legal, and regulatory debates that advance policy priorities for small and mid-market business customers (including QuickBooks, Mailchimp, and Intuit Enterprise Suite).
Intuit, the global financial technology platform that makes TurboTax, Credit Karma, QuickBooks, and Mailchimp, is looking for an innovative and strategic public affairs professional to join our Global Corporate Affairs and Public Policy (GCAPP) team with a specific focus on our Global Small Business Group (GBSG) and Corporate Responsibility policy priorities and advocacy.

DC30+ days ago
p>ITAR REQUIREMENTS:
To conform to U.S. Government export regulations, applicant must be a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder), (iii) Refugee under 8 U.S.C. § 1157, or (iv) Asylee under 8 U.S.C. § 1158, or be eligible to obtain the required authorizations from the U.S. Department of State.
As a member of the SpaceX Government Affairs team, you will support SpaceX and Starlink's business and growth objectives through direct federal lobbying efforts and strategic coalition building on a range of issues, including telecommunications, broadband, and national security.

DC30+ days ago
$200,000–$250,000 Per Year
p>With offices in Toronto, San Francisco, Dallas, and Pittsburgh, Waabi is growing quickly and looking for diverse, innovative and collaborative candidates who want to impact the world in a positive way.
Cultivate and maintain relationships across Congressional offices and committees, and federal Agencies (with a focus on USDOT, NHTSA and FMCSA).

McLean, VA26 days ago
$134,400–$153,300 Per Year
Working for one of the world's most recognized brands that is ranked #106 on the Fortune 500 and #15 on Fortune's 100 Best Companies to Work For, Capital One provides multiple opportunities to learn and grow while engaging with world-class business leaders across the enterprise. This role provides the opportunity to drive policy communications strategies forward in a fast-paced and dynamic external landscape, leveraging best practices across political engagement, reputation management, and campaign advocacy to enable business growth and mitigate risk.

Washington, D.C., Washington, DC30+ days ago
About GKG:
With a passion for excellence, Golden Key Group (GKG) helps clients solve their strategic, organizational, and operational challenges to better meet their mission demands. Overview:
The Program Manager will provide senior-level program management support to the U.S. Department of Veterans Affairs (VA) at VA Headquarters in Washington, DC.

Washington, DC30+ days ago
Remote
$200,000–$230,000 Per Year
You will be responsible for bringing structure, discipline, and clear operating rhythm to a complex, multi state lobbying network, ensuring our external partners are well coordinated, accountable, and aligned to business priorities. We have an exciting opportunity to join our Government & Industry Affairs team in the United States and are currently looking for a Senior Manager, Government & Industry Affairs Operations to join the team.

DC24 days ago
Because many of Radiant's deployments will support national security, energy resilience, and mission assurance objectives across the government (e.g., military, FEMA, and more), this individual will help drive legislative strategies that enable customers to fund, procure, authorize, and scale the deployment of advanced nuclear systems. Portable nuclear power with rapid-deploy capability can replace similar-sized diesel generators and provide critical asset support for hospitals, data centers, remote sites, and military bases.

Washington, DC30+ days ago
$110,700–$185,250 Per Year
Overview The North America Public Policy & Government Affairs (NA PPGA) Communications Manager will play a key role on a high-visibility cross-functional team, responsible for supporting the design and implementation of PepsiCo's North America PPGA Communications strategy and the execution of governmental and external communications, as well as partnering with the pep+ Communications teams. In addition to salary, PepsiCo offers a comprehensive benefits package to support our employees and their families, subject to elections and eligibility: Medical, Dental, Vision, Disability, Health, and Dependent Care Reimbursement Accounts, Employee Assistance Program (EAP), Insurance (Accident, Group Legal, Life), Defined Contribution Retirement Plan.

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Regulatory Affairs Manager Jobs in Washington, DC

Human Resources Manager Shred-Tech Asia Co., Ltd.

Regulatory Affairs Manager AstraZeneca Plc

Regulatory Affairs Manager Katalyst Healthcares & Life Sciences

Policy & Regulatory Affairs Manager Emerald AI

Preferred style="min-height:1.5em">Experience working with or before state Public Utility Commissions and/or the Federal Energy Regulatory Commission (FERC).

Senior Manager Regulatory Affairs US Advertising and Promotion - Immunology AbbVie Inc

Manager, Regulatory Affairs - Advertising and Promotion Supernus Pharmaceuticals Inc

Associate Director/Senior Manager Regulatory Affairs Precigen Inc

Manager, Safety Regulatory Affairs and Certification Mitsubishi Motors North America, Inc.

Regulatory Response Case Manager, Governance and External Affairs Amazon.com Inc

Manager, CMC Vaccines Mature Projects, Regulatory Affairs GSK plc

WHS Regulatory Response Case Manager, Governance and External Affairs Amazon.com Inc

Strategy and Operations Lead, Regulatory Affairs Google LLC

Director, Government & Regulatory Affairs (Hybrid - Washington D.C.,) Broadridge

Vice President, Government, Regulatory, and Public Affairs Modivcare

Vice President, Government, Regulatory, and Public Affairs ModivCare Inc.

Director, Government & Regulatory Affairs (Hybrid - Washington D.C.,) Broadridge Financial Solutions Inc

Attorney-Advisor (Regulatory & Legislative Affairs) U.S. Department of Transportation

Senior Manager, WW Aviation Security Regulatory Affairs, Worldwide Operations Security - Aviation Security Amazon.com Inc

Regulatory Affairs Coordinator - VESPER The Henry M Jackson Foundation for the Advancement of Military Medicine Inc

Director of Regulatory Affairs,Tactical and Implementation Immunocore Holdings Plc

Vice President, Global Head of Regulatory Affairs Qiagen NV

Director of Regulatory Affairs, Satellite Policy Blue Origin Enterprises LP

Vice President, Regulatory Affairs *PC 884 Miltenyi Biotec GmbH

Principal Associate, Chief of Staff - Regulatory Affairs Capital One

Regulatory Affairs Director AstraZeneca Plc

Strategy Lead, CMC Mature, Regulatory Affairs GSK plc

Senior Director, Regulatory Affairs Strategy - Cell and Gene Therapy AstraZeneca Plc

Executive Director, Regulatory Affairs Strategy - Cell and Gene Therapy AstraZeneca Plc

Director, Regulatory Affairs - Neurology MedTech IQVIA

Develop and execute regulatory services for client companies, including however not limited to: Regulatory Submissions (e.g., 510(k), IDE, PMA, IND, BLA, & IND, Technical Documentation, STED, CERs).

Regulatory Submissions (e.g., 510(k), IDE, PMA, IND, BLA, & IND, Technical Documentation, STED, CERs).

Executive Assistant, Government Affairs & Regulatory Viasat, Inc.

Associate Director, Regulatory Affairs US Lead, Regulatory Science & Execution AstraZeneca Plc

Senior Director, Head of US Regulatory Affairs Policy & Intelligence Teva Pharmaceutical Industries Ltd

Executive Director, Regulatory Affairs JPMorgan Chase & Co

Executive Director, Regulatory Affairs Precigen Inc

Government Affairs Director - Global Spectrum Policy & Regulatory Affairs Motorola Solutions Inc

Policy Manager, Copyright, Media, and News, Government Affairs and Public Policy Google LLC

Associate Director, Regulatory Affairs US Lead, Regulatory Science & Execution Alexion Pharmaceuticals Inc

Sr Federal Government Affairs Manager Constellation Energy Generation, LLC.

Campaign Manager, Government Affairs and Public Policy Google LLC

Director, Regulatory Affairs Strategy - Cell and Gene Therapy AstraZeneca Plc

Public Affairs Manager, New Market Development Google LLC

Sr Manager, State Government Affairs - Central The Kraft Heinz Co

Public Affairs Manager - Global Business Solutions Group (GBSG) and Corporate Responsibility Intuit Inc

Government Affairs Manager National Security Space Exploration Technologies Corp

Senior Manager, Federal Policy and Public Affairs Waabi

Policy Communications Manager, Public Affairs Capital One Financial Corp

Program Manager – Veteran Affairs Golden Key Group

Senior Manager, Government & Industry Affairs Operations VGW Holdings Ltd

Senior Manager, Legislative Affairs Radiant Industries Inc

Manager, North America Public Policy Government Affairs (NA PPGA) Communications PepsiCo Inc

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Develop and execute regulatory services for client companies, including however not limited to:
Regulatory Submissions (e.g., 510(k), IDE, PMA, IND, BLA, & IND, Technical Documentation, STED, CERs).