236 Results for

Public Affairs Jobs in California

Jobs

New!

San Francisco, CA1 day ago

$50–$70 Per Hour

Consistently ranked among the nation's best hospitals, particularly recognized for excellence in neurology and neurosurgery; cancer care; heart care; diabetes; ear, nose and throat care; and psychiatry and psychology, among other services. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.

Firebaugh, CA30+ days ago

Finally, Lehigh Valley Hospital - Cedar Crest, Lehigh Valley Hospital - Muhlenberg, Lehigh Valley Hospital- Hazleton, and Lehigh Valley Hospital - Pocono each received an 'A' grade on the Hospital Safety Grade from The Leapfrog Group in 2020, the highest grade in patient safety. We're a Magnet(tm) Hospital, having been honored five times with the American Nurses Credentialing Center's prestigious distinction for nursing excellence and quality patient outcomes in our Lehigh Valley region.

Los Angeles, CA30+ days ago

Westminster, CA30+ days ago

New!

Irvine, CA2 days ago

Remote

$170,000–$190,000 Per Year

The VP partners alongside program leadership and select client stakeholders to collaboratively explore business and talent mobility trends, exchange industry and market perspectives, and co create innovative program strategies and solutions that evolve with the client’s objectives. Additionally, the VP serves as the lead for account integration across operations, advisory, supply chain, and technology, orchestrating seamless collaboration to deliver a cohesive, high‑performing global mobility experience for both the client and their relocating employees.

San Jose, CA9 days ago

Remote

$229,562–$344,342 Per Year

The role oversees a high-impact team and partners cross-functionally and externally to drive an integrated publications and scientific communications strategy, translating complex data into compelling evidence that supports clinical adoption, informs healthcare decision-making, and differentiates the company’s portfolio globally. Agios Pharmaceuticals is searching for a dynamic Senior Director, Global Scientific Communications and Publications expert to join our Global Medical Affairs team and lead a high-functioning communications/publications/congress team.

Sacramento, CA30+ days ago

Full-time

LPA is also a member company of Public Policy Holding Company, Inc., providing us with the unique ability to collaborate with both domestic and international leading government relations and public affairs firms to best serve client needs, and to provide employees with the benefits that come from working in a publicly traded company (London Stock Exchange).Position Overview. Support the supervision and delegation of tasks to junior staff including but not limited to tracking news clips, maintaining and updating key client files, documenting client updates, and other essential client support activities; oversee quality of work deliverables and professional development targets.

New!

Sacramento, CA1 day ago

$151,000–$220,000 Per Year

With the opportunity to initially earn up to 20 days annually plus parental leave, paid holidays, celebration day, life leave (40 hours/year), bereavement leave, and community service/education support days, there will be plenty of time for you! Join State Farm Mutual Automobile Insurance Company-a proud Fortune 50 leader with a legacy of excellence since 1922-as we seek a dynamic and motivated attorney to lead the company's government relations across multiple states.

New!

Orange, CA5 days ago

$70,000–$84,000 Per Year

5 Years experience designing, developing, and implementing large scale training programs; inclusive of project or program management in developing leadership skills, knowledge, and workforce development. See Sharp HealthCare Terms & Conditions at https://www.sharp.com/patient-rights-privacy/terms-of-use.cfm and Privacy Policy at https://www.sharp.com/patient-rights-privacy/privacy-practices.cfm and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions.

San Francisco, CA30+ days ago

$225,000

Strategic Client Leadership & Outcomes - You will serve as the senior strategic contributor to C-suite and executive leaders within the technology sector, guiding them through complex challenges related to corporate reputation, public affairs, and market positioning. We apply our unique expertise across strategic communications, public affairs, research, and digital marketing to create sophisticated and customized strategies that make change possible for both American and European clients.

San Diego, CA19 days ago

$115,000–$155,000 Per Year

In this role, you will act as a primary advisor to leadership, crafting narratives that protect organizational reputation and ensure clear, effective communication across diverse public and private sectors. The Marlin Alliance is seeking a strategic and highly motivated Senior Public Affairs Specialist to lead our mission-critical communications and stakeholder engagement initiatives.

Los Angeles, CA30+ days ago

$76,800–$100,800 Per Year

The Senior Analyst, Government Affairs is a contributor and owner of mission-critical workflows to communicate proposed and enacted legislation, regulations, bulletins, and other regulatory guidance to impacted teams. Support the Government Affairs Counsel with overseeing trade association committees, covering hearings and meetings as assigned by the Government Affairs Counsel and summarizing takeaways for our teams.

Los Angelas, CA30+ days ago

Full-time

Homeboy Industries is the largest gang rehabilitation and re-entry program in the world, providing hope, training, and support to formerly gang-involved and previously incarcerated people, allowing them to redirect their lives and become contributing members of our community. The GAO will write and submit public grant proposals, monitor compliance and reporting requirements, build relationships with key stakeholders to represent Homeboy Industries in grantor monitoring meetings and trainings.

San Diego, CA30+ days ago

Remote

Full-time

Working on a team to help cultivate strategic partnerships with public and private payers, provider organizations, key clinical research institutions, and patient advocacy organizations. Third-Party Ally Development - Similarly, build and lead other disparate advocacy coalition efforts to raise awareness of barriers to patient access to therapy and the importance of fostering a business environment friendly to technology innovation, investment, and employment.

Sacramento, California7 days ago

The Director State Governmental Affairs position is responsible for developing and implementing policy and legislative positions on state and local issues impacting Constellation’s business units and business plans within an assigned region. Review and analyze state legislative and policy initiatives for impact on Constellation positions and recommend actions to senior leadership and communicate and translate state policy positions, key initiatives and implications of legislative and political positions to management.

Sacramento, CA30+ days ago

$169,344–$264,600 Per Year

The responsibilities of the position include, but are not limited to, the following: + Demonstrate a high degree of knowledge about the political, economic, and social factors affecting public policy decision making; how engagement with government officials can lead to the enactment of new or the modification of existing regulations; implement policies and take other governmental actions that are favorable to Chemours’ business growth, corporate well-being, and the industry sectors in which the company operates. The successful candidate will join Chemours’ Global Government Affairs Group with a primary responsibility for supporting U.S. federal regulatory affairs engagement with the United States Environmental Protection Agency (USEPA), as well as other select federal administrative agencies; key trade organizations that help shape regulatory policies at the U.S. federal level; and members of the U.S. Congress and their staffs.

San Diego, CA21 days ago

Proactively identify and create strategic engagement opportunities for the Executive Director and Deputy Executive Director with key funders, stakeholders, community leaders, and partner organizations (briefings, tours, introductions, speaking opportunities, and relationship-building meetings). The Director partners closely with the Deputy Executive Director, Executive Director, Board of Directors, Development Manager, senior leadership, and key stakeholders to grow philanthropic revenue and deepen donor and sponsor relationships.

Richmond, CA30+ days ago

Full-time

Knowledge of current Good ClinicalPractices (cGCP), current Good Manufacturing Practices (cGMP), Good Documentation Practices and a strong understanding of FDA regulations and guidelines. Participate in review of BabyBIG documentation to support highest possible quality of all records produced by manufacturing contractors or contracting research organizations .

La Jolla, CA30+ days ago

$169,700–$282,900 Per Year

Bring strong scientific and communication skills, along with industry knowledge, to support Head of Scientific Affairs and Scientific Affairs team in providing senior-level scientific, strategic and operational support to the Pfizer Chief Scientific Officer (CSO)/President of R&D and Head, Portfolio & Innovation, to create and communicate a compelling scientific narrative for external (investor, others) and internal (Board of Directors - BoD) audiences. Collaborate with the Scientific Affairs team and support the Head of Scientific Affairs in the development of a scientific communications strategy for investors, creating a watchlist of key programs, R&D themes and emerging innovative science, as well as a proactive plan for when and how to communicate them, through a steady cadence of investor events (in collaboration with Investor Relations and Communications).

Mountain View, California30+ days ago

$80,000–$80,000

Ultimate Staffing Services is actively seeking a dedicated and detail-oriented Regulatory Affairs Associate to join a reputable medical device manufacturer. Coordinate, prepare, compile, and maintain regulatory documentation for local and regional registration, license renewal, and product submissions.

Irvine, CA30+ days ago

$50–$54 Per Hour
Contractor

Strict attention to detail Ability to interact professionally with all organizational levels Ability to manage competing priorities in a fast paced environment Must be able to work in a team environment, including inter-departmental teams and representing the organization on specific projects Ability to build productive internal/external working relationships Bachelor's Degree or equivalent in scientific discipline (e.g., Biology, Microbiology, Chemistry) 5-7 years of experience requiredOur client is a leading Medical technology Industry and we are currently interviewing to fill this and other similar contract positions. Coursework, seminars, and/or other formal government and/or trade association training required Proven expertise in Microsoft Office Suite including Word, PowerPoint and Excel Good written and verbal communication skills and interpersonal relationship skills Good problem-solving, organizational, analytical and critical thinking skills Solid knowledge and understanding of global regulations relevant to medical devices, Class II and/or Class III devices Solid knowledge and understanding of global regulatory requirements for new products or product changes.

Irvine, CA30+ days ago

BaRupOn LLC is seeking a highly experienced Director of Licensing & Regulatory Affairs to lead all regulatory strategy, licensing execution, and compliance activities for its Small Modular Reactor (SMR) and Micro Modular Reactor (MMR) programs in the United States. The ideal candidate brings deep, direct NRC engagement experience, a thorough command of U.S. nuclear regulatory frameworks, and the leadership ability to build and manage a high-performing regulatory team in a fast-moving, mission-driven environment.

New!

Irvine, CA4 days ago

Full-time

Education Bachelors degree in Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field Experience 5-7 years of Regulatory Affairs experience in the medical device industry Direct experience supporting Class II medical devices in the U.S. and Class II and/or Class III medical devices EU Handson involvement with EU MDR technical files Shift: [' Ability to manage competing priorities in a fast-paced environment Attention to detail Good problem-solving, organizational, analytical and critical thinking skills Good written and verbal communication skills and interpersonal relationship skills Knowledge and understanding of global regulations relevant to medical devices (Class II and/or Class III)'] Start: [' Proficiency in document management systems and Microsoft Office Solid knowledge and understanding of global regulatory requirements for new products or product changes. Must be able to work in a team environment, including inter-departmental teams and representing the organization on specific projects Ability to build productive internal/external working relationships Coursework, seminars, and/or other formal government and/or trade association training required']

Irvine, CA30+ days ago

$90,000–$127,000 Per Year

Determine and discern detailed requirements on mid-to-large scale projects to establish the project deliverables and develop the project management plan, and manage changes to the project scope, schedule, and costs to keep the project management plan updated and reflective of authorized project changes. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail and technical mastery will help ensure our products reach clinicians and improve patients’ lives.

San Francisco, CA30+ days ago

This role will serve as a key liaison to the medical and scientific community, focusing on building and maintaining relationships with leading experts in pediatric neurology and epilepsy across the West Coast. Minimum of 5 years of experience in the pharmaceutical industry (preferred) as a field-based medical position (MSL or similar) to provide strategic and scientific/medical direction to national/regional business unit functions.

Fremont, CA30+ days ago

The key functions of this role will be to collaborate with internal and external stakeholders including the Foster City Medical Affairs team, Scientific Publications, Medical Affairs Research, Marketing, Global Commercial Product Strategy, Value and Market Access, Clinical Research, Public Affairs, Government Affairs, Contracts/Finance, Pharmacology, Virology and Legal on both the global and regional levels. Excellent analytical and problem solving skills, demonstrated ability to identify and understand complex issues and problems and identify and query key findings from study data and publications.

SF, CA30+ days ago

POSITION SUMMARY:The Senior Regulatory Affairs & Compliance Specialist is responsible for ensuring compliance with regulatory, licensing, and contractual requirements set forth by the Centers for Medicare and Medicaid Services (CMS), the California Department of Health Care Services (DHCS), and other regulatory agencies. Seniors, their family members, and caregivers face many issues, including transportation to appointments, management of medications, coordination of medical care from different specialists, lack of social interaction, and ability to stay alone at home.

Irvine, California23 days ago

$108,100–$156,500 Per Year

Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer. This role directs subordinate supervisors and managers and has organization-wide impact for a variety of functions in graduate student recruitment, admissions, enrolled student services, career counseling, professional development, and graduate advising.

Oakland19 days ago

Remote

Full-time

Working from a strong understanding of AERDF’s model and the broader external landscape, the CEAO will define and execute a comprehensive external affairs strategy, encompassing narrative, brand, fundraising, and stakeholder engagement, to increase AERDF’s visibility, influence, and long-term sustainability. Strategic Planning and External StrategyPartner closely with the Chief Executive Officer and senior leadership team to drive and coordinate AERDF’s multi-year external strategy, aligning external priorities with enterprise goals.

Sacramento, CA30+ days ago

$165,000–$225,000 Per Year

12+ years of biologic or pharma regulatory experience with a Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic or pharma regulatory experience with a Master's Degree in life sciences, quality, regulatory affairs or a related area of study or 7+ years of biologic or pharma regulatory experience with a PhD in life sciences, quality, regulatory affairs or a related area of study. We are focused on the research and development of transplantable kidneys ( mirokidney® ), livers ( miroliver® ), and a bioengineered external liver assist device for acute liver failure ( miroliver_ELAP_® ), with plans to also bioengineer other critical organs like lungs, pancreases and hearts.

New!

Ventura College (Ventura CA), CA4 days ago

The Vice President of Student Affairs has the oversight for functional areas that include: Admission & Records, Articulation, Student Success Plan, Counseling, Educational Assistance Center (EAC), Transfer/Career Center, Extended Opportunities Programs & Services (EOPS), Cooperative Agencies Resources for Education (CARE), CalWORKS, Financial Aid, Student Health Center, International Student Programs, Veterans Affairs, Student Activities, Scholarships, and Outreach and Recruitment. Under the direction of the President, the Vice President of Student Affairs serves as the Chief Student Development Officer and is responsible for the overall design, organization, delivery, supervision, evaluation, and fiscal management of a comprehensive student development program charged with promoting and delivering programs and services that enhance student and staff success, achievement, and retention.

Los Altos, CA30+ days ago

Remote

$140,000

You will operate as a core member of Bidgely’s Regulatory Affairs function, working closely with internal partners across Sales, Go-to-Market, Product, and Engineering to ensure regulatory strategy actively supports customer adoption and market expansion. You will: Monitor and analyze state-level regulatory proceedings, legislation, and utility plans related to grid modernization, data analytics, demand-side management, energy efficiency, and customer experience.

New!

Westminster, CA6 days ago

In this job, you will engage with business units across SCE to develop strategies, business cases, and regulatory deliverables in support of key SCE objectives that require engagement with external regulatory agencies such as the California Public Utilities Commission. You will lead the development of components in the regulatory process, including the full lifecycle from development of testimony, discovery and data requests, hearings, workshops, comments, and final decisions.

Monterey, CA29 days ago

$131,840–$167,890 Per Year

The ideal candidate brings exceedingly strong communication and relationship-building skills, along with the ability to interpret legislative and technical information, translate complex concepts for diverse audiences, and contribute effectively in a fast-paced, policy-driven setting. The Government Affairs Advocate will play a central role in planning and implementing an annual advocacy platform, including tracking and analyzing legislation, monitoring funding opportunities, and engaging with elected officials, partners, and stakeholders to advance M1W's priorities.

Orange, California12 days ago

Proven organizational skills and attention to detail; ability to multi-task, prioritize a complex and dynamic workload, meet rigid deadlines despite interruptions, frequent workload changes and competing demands, and achieve high productivity/quality within short time frames; skill in working independently, taking initiative and following through on assignments and ability to work as part of a team. *Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.

Burlingame, CA30+ days ago

Review significant regulatory issues with manager, as necessary, and resolve submission issues with engineering partners, geography regulatory partners, and regulatory agencies as needed. Interact directly with FDA and/or indirectly with international regulatory agencies on most projects/products at reviewer level.

New!

Arcadia, California2 days ago

$199,000–$285,000 Per Year

General Information: Reporting to the President and CEO and serving on the executive leadership team, the Chief Public Policy Officer (CPPO) provides visionary leadership in public policy, external affairs, and strategic initiatives to advance the agency’s mission, values, and long-term goals. While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to handle, or feel objects, tools or controls; reach with hands and arms; climb stairs; balance; stoop; kneel, crouch or crawl; talk or hear; taste or smell.

Sacramento, CA30+ days ago

$150,000–$200,000
Full-time

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. If you're interested in learning more about this role please send a confidential email with a resume to: https://jobot.com/apply/government-and-regulatory-affairs-attorney/1692133845?utm_source=Monster.

New!

Glendale, CA2 days ago

$39,180–$52,500 Per Year

This role joins a specialized bi-coastal team that works closely with partners across the segment to elevate stories among key advocates and content creators. The base pay actually offered will take into account internal equity and also may vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience among other factors.

New!

Santa Clara, CA1 day ago

$50,000–$200,000 Per Year

Technology moving at the speed of thought" embodies these principles – the need to nimbly utilize the best that information technology offers to meet the business needs of our Federal Government customers. The salary range displayed is an estimate and will be determined based on several factors, including the individual's combination of education, knowledge, skills, competencies, and experience, as well as contract parameters and organizational requirements.

Los Angeles, CA30+ days ago

$18.67–$22 Per Hour

FleishmanHillard was named 2020, 2021 and 2022 Campaign Global PR Agency of the Year; 2023 ICCO Large Agency of the Year – The Americas; 2022 and 2023 PRWeek U.S. Agency of the Year; 2022 and 2023 PRWeek U.S. Outstanding Extra-Large Agency of the Year; 2023 Campaign US PR Agency of the Year; 2021 PRovoke APAC Consultancy of the Year; and 2021 PRWeek UK Large Consultancy of the Year. Our service to clients draws on expertise across more than 25 disciplines, including B2C and B2B marketing, branding, corporate reputation management, CSR, creative services, entertainment and sports, digital and social media, financial communications and investor relations, healthcare, internal communications, issues and crisis management, public affairs, and technology.

San Francisco, CA30+ days ago

$77,000–$175,000 Per Year

FleishmanHillard was named 2020, 2021 and 2022 Campaign Global PR Agency of the Year; 2023 ICCO Large Agency of the Year – The Americas; 2022 and 2023 PRWeek U.S. Agency of the Year; 2022 and 2023 PRWeek U.S. Outstanding Extra-Large Agency of the Year; 2023 Campaign US PR Agency of the Year; 2021 PRovoke APAC Consultancy of the Year; and 2021 PRWeek UK Large Consultancy of the Year. This position is ideal for a strategic advisor and big-picture thinker who is energized by helping enterprise technology companies differentiate not just through AI and product hype, but through authentic storytelling that builds belief with the full constellation of stakeholders that matter: investors, employees, policymakers, talent markets, and society.

Mountain View, CA30+ days ago

$75,000–$95,000 Per Year

Perform and document Complaint Handling, assessment, and reporting Receive and investigate product- and service-related communications / complaints, with communication received from various sources, including communications from field service management platforms (ServiceMax), customer relationship management platforms (SalesForce), enterprise resource planning platforms (Business Central), internal service records, and other direct and indirect customer/user communications. Regulatory Affairs (Associate / Specialist / Senior Specialist) Post Market Surveillance personnel are responsible for: (1) analyzing Post Market Surveillance (PMS) data to prepare Post Market Surveillance reports and documentation, and to update related risk and other documentation accordingly.

Irvine, CA30+ days ago

$145,000–$205,000 Per Year

Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail and technical mastery will help ensure our products reach clinicians and improve patients’ lives. Includes representing the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including providing alternatives for meeting regulatory requirements and resolving complex conflicts between those requirements and development issues.

Los Angeles, CA30+ days ago

$220,000–$250,000 Per Year

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. This role leads high-level, compliant scientific exchange with U.S. payers to ensure Arrowhead's clinical, real-world, and health economic evidence is clearly articulated and aligned with evolving reimbursement expectations.

Sacramento, CA30+ days ago

Remote

$168,000–$231,000 Per Year

The Director of State Public Policy role resides within the Government Affairs Department and will serve as an expert in pharmacy and pharmacist licensure, pharmacy shared services, occupational/facility licensure, PBM, and federal healthcare preemption public policy at the state level while working with subject matter experts and business units across the Humana enterprise. + Represent Humana before national advocacy groups, trade associations, public policy organizations, intergovernmental groups, and state boards of pharmacy/National Associations of Boards of Pharmacy; manage public policy consultants and develop external stakeholder outreach strategies.

San Francisco, CA30+ days ago

$19.13–$30 Per Hour

This may include, but not be limited to, creating and organizing public meeting documentation and materials, attending public events, coordinating with technical teams (e.g., transportation planners, civil engineers, sustainability professionals), implementing social media plans, and communicating with community stakeholders. + Support implementation strategies to engage all communities, especially underserved and marginalized people, impacted by infrastructure projects using a variety of tools and methods (i.e. workshops, public meetings, market research, public information and advertising campaigns, and visuals).

San Francisco, CA30+ days ago

$300,000–$360,000 Per Year

Advance collaborations with Key Opinion Leaders and establish robust partnerships within the medical and scientific community, including oversight of KOL interactions, advisory board strategy, academic partnerships, and professional society activities to generate actionable insights. Provide cross-functional leadership and strategic input across clinical development, clinical operations, regulatory affairs, commercial, market access, and pharmacovigilance to inform product development strategies and commercial planning.

Irvine, CA30+ days ago

$92,000–$130,000 Per Year

Prepare, compile, and support global regulatory submissions for assigned products, including: U.S. submissions (e.g., 510(k)s, IDEs, PMAs, PMA supplements, annual reports) EU submissions under the Medical Device Regulation (MDR) (e.g., Technical Documentation, Design Dossiers, STEDs, clinical evaluation documentation, and responses to Notified Body questions) Support CE marking activities and interactions with Notified Bodies for Class III implantable devices. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail and technical mastery will help ensure our products reach clinicians and improve patients’ lives.

Irvine, CA30+ days ago

$72,000–$102,000 Per Year

Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail and technical mastery will help ensure our products reach clinicians and improve patients’ lives. + Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving conflicts between those requirements and development issues, and/or reporting to management.

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Public Affairs Jobs in California

Jobs

Labor & Employee Relations RepresentativeJobot

Child Life Specialist - FT Days - Pediatrics and PICU - FirebaughLehigh Valley Health Network

Child Life Specialist - FT Days - Pediatrics and PICU - PalmdaleLehigh Valley Health Network

Child Life Specialist - FT Days - Pediatrics and PICU - WestminsterLehigh Valley Health Network

Vice President of Client Relations - Global Engagements (Remote)Weichert, Realtors

Senior Director, Global Scientific Communications and Publications - RemoteAgios Pharmaceuticals

Director, Public AffairsLucas Public Affairs

Legislative/Regulatory CounselState Farm Mutual Automobile Insurance Company

Program Manager - The Sharp University Learning Programs - Full Time - HybridSHARP HEALTHCARE

Managing Director, Public Affairs & Strategic Communications (Technology)Bully Pulpit International

Senior Public Affairs/Communications SpecialistThe Marlin Alliance

Senior Analyst, Government AffairsOscar

Government Affairs Grant OfficerHomeboy Industries

Director, Federal Government Affairs (Washington D.C./Remote)Illumina, Inc.

Director, State Govt Affairs - California/WestConstellation Energy Generation, LLC.

Regulatory Affairs Director (US)Chemours

Director of Development & External AffairsMission Edge San Diego

Regulatory Affairs CoordinatorPublic Health Foundation Enterprises, In

Director, Scientific AffairsPfizer

Regulatory Affairs AssociateJess Bushey

Coord 3, Regulatory AffairsPyramid, Inc

Director of Licensing & Regulatory Affairs (SMR / MMR Programs)BaRupOn LLC

Coord 3, Regulatory AffairsLanceSoft Inc

Senior Analyst, Project Management, Regulatory Affairs SurgicalEdwards Lifesciences

Associate Director, Medical Affairs, West CoastTaylor Strategy Partners

Global Medical Affairs ManagerCEDENT

Snr Regulatory Affairs & Compliance Specialist PACEOn Lok

Graduate Division Assistant Dean, Academic and Student AffairsUniversity of California, Irvine

Chief External Affairs OfficerAERDF

Associate Director, Regulatory AffairsUnited Therapeutics

Interim Vice President of Student AffairsVentura County Community College District, CA

Manager, Regulatory Affairs & Market DevelopmentBidgely Inc.

Utility Regulatory Affairs Senior AdvisorSouthern California Edison

Government Affairs AdvocateWBCP, Inc.

Regulatory Affairs CoordinatorUniversity of California, Irvine

Medical Devices, Regulatory Affairs SpecialistMeta

Chief Public Policy OfficerPacific Clinics

Government and Regulatory Affairs AttorneyJobot

Associate, Public Relations (Casual Temporary/Seasonal)The Walt Disney Company

Department of Veteran Affairs VA NEDIISTekSynap

Influencer/Public Relations Intern (Full-Time) - Los Angeles, Spring 2026FleishmanHillard

Vice President - Tech Advisory Public RelationsFleishmanHillard

Regulatory Affairs - Post Market SurveillanceIridex Corporation

Senior Manager, Regulatory Affairs TMTTEdwards Lifesciences

Director, Medical Affairs PayerArrowhead Pharmaceuticals

Director, State Public PolicyHumana

Communications & Public Involvement Intern - Summer 2026WSP USA

Vice President, Medical AffairsVir Biotechnology

Senior Specialist, Regulatory Affairs SurgicalEdwards Lifesciences

Specialist, Regulatory Affairs THVEdwards Lifesciences

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