Regulatory Affairs Specialist
$120k - $150kPivotal
Pivotal eVTOL Aircraft Certification Strategy ManagerPivotal is the leader in the emerging market of electric Vertical Takeoff and Landing (eVTOL) aircraft. We design, develop, and manufacture light eVTOL aircraft and are renowned for the BlackFly aircraft the world's first light eVTOL to fly manned missions and enter the consumer market. Efficient, compact, and simple, Pivotal aircraft are designed for a wide range of consumer, public service, and defense applications. Our distinctive tilt-aircraft architecture and scalable platform have been flying for over 10 years. Last year we announced our next-generation aircraft, the Helix, which is rapidly progressing toward general release and scalable production in early 2026. Mobility is one of the most highly-valued areas of modern technology investments. This is the right company, in the right space, the right strategy, at the right time. If you are ready for adventure, we invite you to join our amazing team and grow with us.Responsibilities:Lead certification pathways across FAA frameworks (e.g., Part 103, Part 21, Part 23, MOSAIC, experimental and special airworthiness categories)Develop and maintain certification roadmaps aligned with product and business strategyDraft and manage applications for: Exemptions, Special Airworthiness Certificates, Waivers & COAsPartner closely with engineering and flight test teams to ensure compliance alignment early in designRegulatory EngagementServe as primary Pivotal representative to: Aeronautical Authorities including FAA (and offices including AIR, AFS, FSDOs) and as well as international civil aeronautical authoritiesSupport communication with FSDOs and other regulators, including proactive outreach and issue resolution.Prepare briefing materials, white papers, and engagement strategies for regulatorsSupport and lead regulatory meetings, early engagement sessions, and auditsGlobal Market EntryIdentify and execute pathways to enter new markets internationallyAssess regulatory environments and define certification/operational strategies for each regionBuild relationships with local regulators and industry bodiesEnable scalable approaches (e.g., training local maintainers, operational approvals, public-use pathways)Regulatory Intelligence & ForesightStay ahead of evolving regulations (FAA MOSAIC, AAM frameworks, international equivalents)Drive Pivotal priorities with regulators while charting a way to actionable company regulations strategyAdvise leadership on risks, opportunities, and timing implicationsBenchmark best practices across the industryOperational SupportDraft regulatory-facing documentation for executive reviewSupport development of: Operating manuals, CONOPS, Training frameworksEnable programs like EMS, public-use operations, and pilot deploymentsQualifications:5+ years in aviation regulatory, certification, or airworthiness rolesDeep experience with FAA certification processes (Part 21, Part 23 strongly preferred)Familiarity with emerging aircraft categories (eVTOL, ultralight, experimental, UAS)Experience engaging directly with FAA, FSDOs, DERs, or ODA unitsStrong working knowledge of international certification frameworks (Transport Canada, EASA, CAA, etc.)Ability to operate both strategically and tactically (write + execute)Preferred Qualifications:Experienced Aeronautical Engineer or Mechanical Engineer with a history of driving technical standards on ASTM or similar organizations.Experience with exemptions, public-use operations, or novel regulatory pathwaysBackground in startups or fast-moving environmentsNetwork within FAA or global aviation authoritiesAttributes Aligned with Core Values:Demonstrates a proactive safety mindset by embedding safety into daily operations, identifying and mitigating risks through assessments and training, encouraging open dialogue on safety concerns, and continuously improving protocols to ensure a safe work environment.Puts customers at the center of every action by deeply understanding their challenges, delivering exceptional value, and striving to exceed expectations to support their success as our core purpose.Actively seeks and values diverse stakeholder perspectives, builds cross-functional relationships, and fosters trust through empathetic, fact-based communication—committing to shared decisions for the greater good.Drives results with clarity and purpose by focusing on what matters most, adapting to change, taking initiative, and owning outcomes while aligning actions with a clear understanding of success at every level.Navigates ambiguity with resilience and bold thinking, challenges the status quo, and combines innovative ideas with practical best practices to overcome obstacles and drive progress.Fosters a high-performance culture grounded in respect, professionalism, and support—balancing high expectations with a healthy, collaborative environment and being a trusted, dependable teammate.$120,000 - $150,000 a yearPivotal offers a comprehensive benefits package, including medical, dental, vision, and 401k plans.Pivotal is an Equal Opportunity Employer. Pivotal does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.Applicants must be eligible for employment in the United States and willing to work onsite at our HQ office in Palo Alto, CA.
$145k - $167k
...relevant diagnostic imaging. Learn MoreAbout The RoleJob Title: Senior Regulatory Affairs SpecialistLocation:Palo Alto, CA or Guilford, CT (Hybrid, 3 days/week)The Senior Regulatory Affairs Specialist advises regulatory strategy for the company’s devices and ensures...SuggestedWork experience placementWork at officeWorldwideWork visaNight shiftWeekend work3 days per week$55 - $60 per hour
...Job Title: Sr. Regulatory Affairs Specialist Location: Sunnyvale, CA, United States Type: Contract Compensation: $55.00 - $60.00 Work Model: Hybrid Overview Established Medical Device company is looking to hire a Sr. Regulatory Affairs...SuggestedContract workLocal area- ...Regulatory Affairs Specialist 4Our client, an American Biotechnology company, is looking for a Regulatory Affairs Specialist 4 for their Sunnyvale, CA/Hybrid location.Responsibilities:Provide regulatory guidance to product teams, develop regulatory plans, and review and...Suggested
- ...The Senior Regulatory Affairs Specialist leads regulatory operations activities with a focus on global tender support, regulatory documentation, and post-approval regulatory activities. This role is responsible for ensuring timely, compliant, and high-quality regulatory...Suggested
$50 - $55 per hour
...Trade Compliance Specialist Base Pay Range $50.00/hr - $55.00/hr Employment Type Contract Seniority Level Mid‑Senior level Location Palo Alto, CA 94304 (Onsite) Role Summary Client is seeking an experienced and adaptable Interim Trade Compliance Specialist for a 6‑month...SuggestedFull timeContract workTemporary workInterim roleLocal areaImmediate start$171k - $231.4k
...tablets, Fire TV and Echo Frames. Working as part of the Medical Devices Operational Compliance Team (MD-OCC), the Sr. Regulatory Affairs Specialist will be working to build best in class products.The ideal candidate will have experience building a regulatory strategy...For contractorsLocal areaFlexible hours$100k - $200k
...States - California - Santa ClaraJob Type: Full timeCategory: Regulatory AffairsIndustry: HealthcarePosted Date: 2026-08-26Abbott is... ...a highly motivated and experienced Principal Regulatory Affairs Specialist to join our Vascular Division team on-site in Santa Clara, CA...For contractors$81.5k - $141.3k
...States - California - Santa ClaraJob Type: Full timeCategory: Regulatory AffairsIndustry: HealthcarePosted Date: 2026-07-01Abbott is... ...Abbott is seeking a passionate, experienced Regulatory Affairs Specialist to join our Vascular Division team on-site in Santa Clara, CA...For contractors$115.86k - $133.01k
...Transfer and Tangible Research property Agreements, draft language that complies with University, Federal and other sponsors and other regulatory policies, requirements, and conditions. Negotiate other research‑related agreements that involve intellectual property,...Hourly payFull timeContract workCasual workWork at officeRemote work$90k - $180k
...0 people with diabetes from routine fingersticks. The Opportunity As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment...Work experience placementWorldwideShift work$90k - $180k
...balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.This Senior Regulatory Affairs Specialist position is an on-site opportunity working out of our Santa Clara, or Temecula, CA locations in the Abbott Vascular Division...WorldwideShift work- ...Function of Position This role provides expert support for regulatory project management, strategic submissions, and cross-functional... ...labeling and documentation. • Mentor and coach regulatory affairs specialists. • Track and report metrics on regulatory timelines and...Local areaWorldwideFlexible hours
$34 - $44 per hour
DescriptionA client with Kforce is seeking an IT Risk and Compliance Analyst I to join their team in Mountain View, CA.Summary:The client's Trust and Safety team harnesses the power of data, technology, and people to protect our customers, partners, and business from fraud...$55 - $60 per hour
...Job Title: Regulatory Affairs Specialist IV Location: Sunnyvale, California Type: 6 month contract Compensation: $55-60/hour depending on qualifications Work Model: Hybrid – 3 days onsite Hours: 40.0 Overview Lead regulatory strategy and submissions...Contract workTemporary workLocal area$97k - $114k
...Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China’s National Medical Products... ..., and Ireland. Overview of Role: The Associate of Regulatory Affairs will support the day-to-day regulatory activities of assigned...$97k - $114k
...Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China’s National Medical Products... ...and Ireland. Overview of Role: The Associate of Regulatory Affairs will support the day-to-day regulatory activities of assigned...Contract workFor contractorsFor subcontractor- ...team as well as the Product Localization Engineering (PLE) and other cross‑functional supporting teams, make sure the company's regulatory affairs activities are conducted in accordance with company policies and in compliance with the latest relevant regulations and...For contractorsLocal areaWorldwideFlexible hours
$25 per hour
...Description Job Description Job Title: Field Action Quality Specialist Location: Sunnyvale, CA Type: 6 month contract... ...role serves as a key liaison between customers, quality teams, regulatory functions, and cross-functional stakeholders to ensure timely...Contract workFor contractorsLocal area- Veterans Health Administration is seeking an Equal Employment Opportunity Specialist to assist the EEO Manager in planning, development, implementation, evaluation, and monitoring of affirmative action and equal employment opportunity programs within the VA Palo Alto Health...
$260k - $360k
...details A renowned interdisciplinary life sciences and healthcare regulatory practice seeks a mid-level associate to advise sophisticated... ...white collar, transactional, intellectual property, and other specialist teams. Conduct sophisticated legal research, draft client...Work at officeLocal areaRemote workFlexible hours- Ropes & Gray LLP is seeking a Conflicts Analyst to support the firm’s risk management by researching and reporting conflicts as they relate to new matters, lateral hires and other routines. This non-exempt, hybrid role is based in the firm’s US offices with hours 12:00 ...
- Cooley LLP in Palo Alto is seeking a Senior Conflicts Analyst (New Business) to identify, analyze, and resolve conflicts for engagements and hires, using independent judgment and knowledge of professional conduct. You will prepare reports, conduct corporate research, and...
- ...no exceptions Role Summary The Import Compliance Specialist will provide hands-on import compliance support, focusing on tariff... ...compliant records and documentation in accordance with regulatory requirements. Ensure regulatory compliance by staying updated...
$110k - $125k
A leading tech company in the San Francisco Bay Area is seeking a Senior Trade Compliance Classification Analyst to efficiently manage import/export compliance. The role requires extensive knowledge of U.S. Customs regulations and a proactive approach in resolving customs...$110k - $125k
...Classification Analyst Duration: 5+ Months Role Summary RV Tech is seeking an experienced and adaptable Interim Trade Compliance Specialist. This individual will serve as a critical stop‑gap, immediately alleviating the urgent operational workload associated with...Full timeInterim roleImmediate start- ...Job Overview A law firm seeks a Healthcare Regulatory Associate in Palo Alto. This role offers the opportunity to work on health innovation, representing companies from pre-formation to capital markets, including public health tech companies. Duties Advise on healthcare...Flexible hours
- ...that can significantly restrict daily activities and negatively impact quality of life. Position Overview The Principal Regulatory Affairs Specialist drives the full spectrum of regulatory activities, from initial market authorization through post-market compliance, for...
- ## Principal Regulatory Affairs SpecialistApplylocations: California - Headquarterstime type: Full timeposted on: Posted 4 Days Agojob requisition... ...That Awaits You:**The Principal Regulatory Affairs Specialist provides regulatory leadership for product manufactured by PROCEPT...Work at office
- ...Join a pioneering MedTech company that's transforming cardiac care with innovative solutions. The client seeks a Principal Regulatory Affairs Specialist to lead complex regulatory strategies and submissions for Class III implantable devices and software-driven technologies...
- ...Sr. Regulatory Affairs SpecialistWe are searching for an experienced regulatory professional to work within the Companion Diagnostics (CDx) team. Reporting to the Sr. Director, Regulatory Affairs (CDx), the successful candidate must have global regulatory experience working...
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