36 Results for

International Affairs Jobs in Los Altos, CA

Jobs

New!

San Jose, CA4 days ago

Remote

$183,549–$275,324 Per Year

The current base salary range for this position is expected to be between $183,549 – $275,324 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. As a key cross-functional partner, the Medical Director collaborates closely with Commercial, Clinical Development, Regulatory, and Market Access teams, among others, to shape brand and portfolio strategy, integrating real-world evidence and external expert perspectives.

New!

San Jose, CA5 days ago

$32–$32

Apply quickly and efficiently online • Weekly pay and Daily Pay Options• Competitive benefits See a different world.“Securitas is committed to diversity, equity, inclusion and belonging in the workplace. Bachelor’s degree in Information Technology, International Affairs/Relations/Business, Emergency Management, Political Science, Criminal Justice or related discipline.

San Jose, CA27 days ago

Education: Bachelor’s degree in Business, International Trade, Supply Chain, or a related field; • Experience: 6-10 years of experience in trade compliance, import/export operations, or customs, preferably in a multinational environment. This position is ideal for mid- to senior-level trade compliance professionals to join the Global Trade Compliance (GTC) team as a Senior Analyst, Trade Compliance and Sanction Screening, North America.

New!

San Francisco, CA4 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.

San Francisco, CA30+ days ago

Remote

$40,000–$45,000

As a junior analyst, you will work closely with senior team members to support research projects, analyze data, and compile reports that assist in decision-making for our diverse range of clients. In this role, you will play a vital part in analyzing global trends, political developments, and economic conditions to provide insights that inform our consulting strategies.

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.

New!

South San Francisco, CA6 days ago

Remote

$170,000–$210,000 Per Year

Reporting to the Senior Director, Regulatory Affairs, this position will serve as a core regulatory representative on cross‑functional program teams, supporting interactions with global health authorities and ensuring regulatory strategies and submissions are aligned with evolving regulatory expectations for cell and gene therapies. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.

New!

South San Francisco, CA2 days ago

$89.68–$122.97

The ideal candidate will possess strong business acumen, experience supporting enterprise platforms such as Salesforce CRM, and the ability to collaborate effectively with IT, analytics, digital, and global business teams. Job Summary We are seeking an experienced Business Analyst with strong expertise in Medical Affairs systems, analytics, and cross-functional collaboration within the pharmaceutical industry.

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.

Santa Clara, CA30+ days ago

Full-time

Act as a strategic partner with medical evidence generation colleagues in Preclinical Research, Clinical Development, and Health Economics Market Access teams to develop and execute global strategies for evidence generation for new and existing products to support regulatory approval/clearance, health technology assessment, customer access, and post-marketing support. Minimum of 7+ years relevant experience in post-graduate medical education ( beyond initial licensure ) including: specialty residency, fellowship or subspecialty training, clinical practice, dedicated research, or other related training/experience in Interventional Pulmonology required.

Pleasanton, CA30+ days ago

Remote

$145,000–$165,000 Per Year

This leadership role within Medical and Clinical Affairs is responsible for strategic management of Scientific Affairs activities including scientific communications, publication and podium planning, KOL engagement and pre-clinical evidence generation. Management of various research related projects including but not limited to clinical pipeline deliverables, regulatory submissions, pre-clinical experimentation, competitive intelligence gathering and databased analyses .

Palo Alto, CA30+ days ago

$145,000–$167,000 Per Year

Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop®system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of care in a healthcare facility. Assess and advise regulatory strategies to optimize business expectations related to domestic and international commercial product availability and regulations:Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop solutions.

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.

Pleasanton, CA30+ days ago

$120,000–$140,000 Per Year

The Scientist, Scientific Affairs is an integral member of the Medical and Clinical Affairs team and will lead and/or participate in several dynamic workstreams including but not limited to scientific communication strategy, support of clinical and R&D initiatives, regulatory submissions and marketing priorities. Marketing Initiatives Collaborate with the marketing team to translate scientific data into compelling marketing messages and develop scientific content for promotional materials as needed.

South San Francisco, CA30+ days ago

$276,000–$345,000

Collaborate with cross-functional teams (Clinical Development, CMC, Quality Assurance) to ensure regulatory compliance throughout the development process and ensure cross-functional alignment during key steps across multiple projects simultaneously. We are seeking a strategic and results-oriented leader to oversee all regulatory activities for our hematology/immunology pipeline, with an initial focus on the upcoming Phase 3 clinical trial for our lead candidate, VGA039.

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.

Mountain View, CA30+ days ago

$110,000–$160,000

O Actively communicate with key suppliers to find if any procurement related (lead time, delivery schedules, etc.) issue occur. O Actively source new technology partners following our internal scouting framework.

San Francisco, CA22 days ago

Minimum three years cumulative recent experience in business development or program management, such as client and stakeholder relationship management, business development (including cold outreach), project management (planning, reporting, budgeting), research and analysis, strategic advice, briefing and report writing for senior audiences. TIOs are results-driven and focused on advancing Ontario’s commercial interests through three core pillars: (1) export promotion, (2) foreign direct investment attraction, and (3) supporting commercial research and development partnerships.

San Francisco, California24 days ago

$80,000–$90,000 Per Year

San Jose, CA30+ days ago

$141,200–$194,200 Per Year

Education: Bachelor’s degree in Business, International Trade, Supply Chain, or a related field; Experience: 6-10 years of experience in trade compliance, import/export operations, or customs, preferably in a multinational environment. Flexible Spending Accounts– Employees may be eligible to participate in a health care account (including a limited health FSA if enrolled in a HDHP), dependent care account, and a pre-tax commuter benefit plan.

San Francisco, CA22 days ago

In order to perform the duties relevant to this job, the following experience is required: Minimum of one (1) year of cumulative experience providing administrative or operational support services in an office environment, including coordinating tasks (e.g., scheduling meetings, organizing travel, supporting events); Preparing and reviewing documents, correspondence or reports, and maintaining records, databases or filing systems. TIOs are results-driven and focused on advancing Ontario’s commercial interests through three core pillars: (1) export promotion, (2) foreign direct investment attraction, and (3) supporting commercial research and development partnerships.

South San Francisco, CA19 days ago

$336,000–$405,000 Per Year

Reporting to the Chief Medical Officer (CMO), the Vice President, Clinical Development provides executive leadership for the company’s clinical research and development activities within designated therapeutic areas and/or programs. The Vice President, Clinical Development serves as a senior leader within Clinical Development, accountable for clinical trial execution, data integrity, regulatory readiness, and cross-functional alignment.

Palo Alto, CA24 days ago

Palo Alto Veterans Institute for Research (PAVIR) is seeking a full-time Clinical Research Assistant to work under the guidance/direction of VAPAHCS Principal Investigator (PI) - Dr. Minal Vasanawala - while supporting different aspects of the clinical research program in Nuclear Medicine Service, which includes facilitating clinical trials from inception to closeout. PAVIR engages in the administration of funds and providing support for the conduct of research at the Veterans Affairs Palo Alto Health Care System (VAPAHCS) to find new and improved ways to combat human disease and help people with disabilities.

Palo Alto, CA30+ days ago

$80,000–$100,000 Per Year

As a Data Labeling Specialist, you will work as part of a collaborative team to label video, text, and imagery (primarily overhead) at a pace that meets our client deliverable deadlines and quality requirements. Cultivate expertise and leadership in the imagery analysis domain and gain basic machine learning knowledge to better understand how labels are utilized by our algorithms.

South San Francisco, CA8 days ago

Remote

$200,000–$250,000 Per Year

Drive Medical Communications (MC) for assigned pipeline assets in partnership with internal stakeholders and external vendors/agencies, including development of the scientific platform and creation/review of scientific communication deliverables (e.g., slide decks, congress materials, FAQs, field medical materials) through MRC review and warehousing. This role will be accountable for defining and executing the global medical information and scientific communications strategy, establishing operational excellence, and ensuring compliant, high-impact scientific exchange aligned with Allogene’s mission to advance allogeneic CAR-T therapies for patients with serious diseases.

New!

Cupertino, CA1 day ago

This contractor will work directly alongside Client's CMM Global Supply Manager to co-drive two parallel workstreams: driving structured raw material risk mitigation best practices with suppliers and engaging suppliers to reduce raw material risk exposure. Operations Platforms: Comfortable working in or learning digital platform tools to manage multi supplier tracking systems, build structured databases, and maintain live program dashboards.

Santa Clara, CA30+ days ago

$86,700–$173,300 Per Year

The primary function of a SENIOR CLINICAL EVALUATION SCIENTIST/PROJECT MANAGER is to combine understanding of scientific and research methodology, medical device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking of new devices and maintaining of CE Mark for existing devices in accordance with MEDDEV 2.7/1 Rev 4, MDD, AIMDD, MDCG Guidance documents, and EU MDR 2017/745. + Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D Engineering, Clinical Engineering, A&P and Marketing, Library Services, Quality Engineering, Post-market Surveillance Group, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers).

Santa Clara, CA30+ days ago

$144,010–$301,610 Per Year

Job Type: Experienced HireShift: Shift 1 (United States of America)Primary Location: US, California, Santa ClaraAdditional Locations: US, Arizona, Phoenix, US, California, Folsom, US, Oregon, Hillsboro, US, Washington, D.C.Business group: Intel’s Corporate Affairs, Policy, Integrity, Trade, and Legal (CAPITL) group offers unique opportunities to work in a variety of areas, including counsel to Intel businesses; technology and intellectual property licensing; patent prosecution; trademarks and brands; litigation, mergers, acquisitions and investing; public policy, legislative and regulatory lobbying; global trade, export, import, and customs; and corporate compliance. As part of the Americas ECSC team, this position involves close collaboration with ECSC colleagues in Asia and Europe, while engaging regularly with business leaders, legal counsel, industry partners, and government officials to ensure seamless compliance operations.

Palo Alto, California16 days ago

$186,000–$232,500 Per Year

New!

Mountain View, California3 days ago

$140,000–$250,000 Per Year

Identify, evaluate, and present findings related to adversarial financial and business relationships surrounding early stage vendors to publicly traded companies involved in emerging tech sectors, to include diligence on capital providers, defense-related academic grants, and other related entities. business administration, business management, law, international relations, economics, criminology, or a related discipline); or public policy discipline relevant to the field of national security; or, 10-20 years of successful business experience or professional field experience and impact considered in lieu of both undergraduate and advanced degrees.

Pleasanton, CA30+ days ago

$200,000–$230,000 Per Year

Responsible for overseeing, planning, leading and driving activities such as Risk Management, Biocompatibility, Shelf-Life Studies, Test Method Validation, Reliability Engineering, and Statistical Analysis in support of new product development, product changes, and sustaining product engineering. The Director, Design Quality Assurance provides strategic representation, planning, management, direction, and guidance to meet quality engineering goals and objectives supporting new product development and sustaining commercial products.

Pleasanton, CA30+ days ago

$155,000–$195,000 Per Year

In this position, this person will work in conjunction with the Operations and R&D functions in selecting, managing and maintaining the supply base, driving acceptable supplier performance, pursuing supplier improvement activities/initiatives, and implementing and overseeing strategic supplier management programs such as Supplier Certification, Alternative Inspection Methods, Supplier Performance and Recognition, and Continuous Improvement initiatives. Overall responsible for developing, implementing, maintaining, and overseeing all aspects of Calyxo's Supplier Quality Engineering program and ensuring the necessary systems, procedures, and processes are established to support both current and future business needs.

Newark, CA30+ days ago

$270,000–$330,000 Per Year

This role will lead the GMP batch review, disposition, CMO deviations and change management programs for API, drug product and finished goods as well as lead all aspects of Quality Analytical including the annual stability program, release testing, trending of data, method validation, compliance and oversight of contract test labs and laboratory out of trend and out of specification investigations. Establish data trending programs across products to proactively identify and investigate trends and report trending outcomes at Quality Management Review and other forums.

Santa Clara, CA30+ days ago

$50,000–$70,000 Per Year

Identifies and controls Manufacturing process defects (scrap, nonconforming material, customer complaints) by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. Leads process improvement efforts by identifying methods to capture quality metric data and by performing appropriate analysis methods to enhance sustaining product design and new product development.

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International Affairs Jobs in Los Altos, CA

Jobs

Medical Director, Global Medical Affairs - RemoteAgios Pharmaceuticals

Global Security Operations Center (GSOC) Operator.Securitas

Senior Analyst, Trade Compliance & Sanction ScreeningAlign Technology, Inc.

Senior Director, Global Scientific Communications and Publications - RemoteAgios Pharmaceuticals

International Affairs Analyst (Remote)Amyand Consulting

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

Associate Director, Regulatory AffairsAllogene Therapeutics

Business Analyst – Medical Affairs Systems & AnalyticsInfobahn SoftWorld Inc

Regulatory Affairs AssociateJess Bushey

Director, Medical Affairs (Monarch Flexible Robotics)Johnson and Johnson

Manager, Scientific Affairs- Remote, USACalyxo

Senior Regulatory Affairs SpecialistHyperfine

Medical Devices, Regulatory Affairs SpecialistMeta

Scientist, Scientific Affairs - Pleasanton, CACalyxo

VP. Regulatory AffairsStar Therapeutics

Global Medical Affairs ManagerCEDENT

International Procurement Center Manager, bilingual KoreanCesna Recruitment

Commercial Officer (Ontario)Global Affairs Canada Locally Engaged Staff Recruitment /Affaires mondiales Canada Dotation des employés recrutés sur place

Associate Director, Law Enforcement and Community Security Partnerships, West DivisionAnti-Defamation League

Sr. Analyst, Trade Compliance & Sanction Screening, North AmericaAlign Technology

Commercial Assistant (Ontario)Global Affairs Canada Locally Engaged Staff Recruitment /Affaires mondiales Canada Dotation des employés recrutés sur place

Vice President, Clinical DevelopmentRigel Pharmaceuticals, Inc.

Clinical Research Assistant – Nuclear Medicine ServicePAVIR

Data Labeling SpecialistRhombus Power, Inc.

Director, Global Medical Information & Scientific CommunicationsAllogene Therapeutics

Supply Risk ManagementIconma

Senior Clinical Scientist - Project ManagerAbbott

Senior Export Compliance SpecialistIntel

Manager, ADS Safety Case, RegulatoryRivian

Business Intelligence Program ManagerRiverside Research Institute

Director, Design Quality Assurance - Pleasanton, CACalyxo

Manager, Supplier Quality Engineer - Pleasanton, CACalyxo

Executive Director, Quality OperationsArdelyx, Inc.

Quality EngineerSEDAA

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