1,467 Results for

Director Of Regulatory Affairs Jobs in California

Jobs

West Hollywood, CA

$120,000–$145,000 / year
Full time

Oversee product testing processes, including sample coordination, protocols, vendor quotes, and method validation to ensure accuracy, reliability, and regulatory compliance of testing procedures. We are seeking a highly detail-oriented QA & Regulatory Sr Manager to oversee product compliance, safety, and quality systems across the full product lifecycle.

24 days ago

Oakland, CA

$115,000–$130,000 / year

Through partnerships with global supply chains and community organizations, SupplyBank.org provides a highly cost-effective and scalable mechanism for bulk purchasing and efficiently distributing necessary health, education, and emergency supplies to children, families, and communities that need them throughout California. This role is approximately 80% focused on Oakport — a transformative shoreline restoration, environmental resilience, infrastructure, and nonprofit campus project in Oakland — and 20% focused on broader SupplyBank.org policy, advocacy, and public-sector initiatives.

1 day ago

El Segundo, CA

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Craft a modern regulatory strategy based in sound engineering principles with input from executives, our board of directors, and industry experts that brings the safest product to market the fastest. 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.

24 days ago

Thousand Oaks, CA

$255,302–$345,408 / year

p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

30+ days ago

El Segundo, California

li>

Craft a modern regulatory strategy based in sound engineering principles with input from executives, our board of directors, and industry experts that brings the safest product to market the fastest. . 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.

28 days ago

Alameda, California

p style="min-height:1.5em">We’re looking for a Director of Regulatory Affairs for our office in Alameda, California who wants to lead, develop and execute the regulatory strategy for Epia Neuro’s Class III implantable neurotechnology.

Lead the execution of regulatory submissions end-to-end, driving the development of BDD, Q-Subs, IDE, and PMA deliverables through hands-on leadership and strong cross-functional coordination.

30+ days ago

San Diego, CA

$180,000–$210,000 / year

Oversee preparation of regulatory documents including: Regulatory briefing documents for U.S. and international health authority meetings Nonclinical/toxicology summaries Clinical protocols Investigator Brochures Annual reports and safety updates Coordinator global submission timelines and ensure consistency across regulatory dossiers Ensure high-quality, compliant regulatory documentation aligned with FDA and ICH guidance. The Director will be responsible for regulatory submissions (including INDs), regulatory reporting for preclinical and clinical programs, orphan and fast track designation applications, oversight of toxicology reporting, and development of integrated regulatory strategies aligned with long-term development and commercialization goals.

30+ days ago

Sacramento, CA

$148,085–$174,000 / year

In this role, you will facilitate coordination across offices and disciplines, share regulatory updates and best practices, support staff training, and partner with Government Affairs and regional leadership on policy developments, draft legislation, and emerging issues that may affect RES business lines and environmental markets. This position is ideal for a seasoned regulatory leader who brings deep expertise in environmental permitting, restoration and mitigation strategy, agency coordination, technical review, staff development, and cross-functional project leadership.

30+ days ago

Irvine, CA

p>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.

30+ days ago

Redwood City, California

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Lead global regulatory strategy from candidate selection through end-of-Phase 2.

Shape early clinical development strategy by providing regulatory leadership on dose-finding approaches and indication selection that enable accelerated and differentiated development pathways and position asset for global registration and Health Authority Engagement. The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.

30+ days ago

Redwood City, CA

$244,000–$305,000 / year

ul>

Lead global regulatory strategy from candidate selection through end-of-Phase 2.

Shape early clinical development strategy by providing regulatory leadership on dose-finding approaches and indication selection that enable accelerated and differentiated development pathways and position asset for global registration and Health Authority Engagement. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.

30+ days ago

Pasadena, CA

$180,000–$200,000 / year

ul>

Provide regulatory review and strategic guidance for promotional (branded and disease state) and medical communications for US prescription drug products across multiple channels, including digital, social media, websites, emails, print, speaker programs, video testimonials, scientific congresses, and field communications, among others. 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.

2 days ago

San Diego, CA

Remote

$130,000–$250,000 / year

The Early Research and Development Group (ERDG) and the Advanced Research and Development Group (ARDG) at Mapp Biopharmaceutical are responsible for the execution of high quality Research and Development activities to ensure the achievement of a robust portfolio through CMC, Nonclinical, Regulatory, Project Management, and Clinical activities consistent with Mapp's product development objectives. Mapp Biopharmaceutical, Inc. "Mapp" is a San Diego based, innovative biopharmaceutical company focused on addressing unmet medical needs through the development of life-saving monoclonal antibody treatment options to combat a variety of neglected and tropical infectious diseases, and in support of biodefense programs.

10 days ago

Mountain View, CA

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Evaluate potential or emerging internal and external risk and proactively undertake and strategically manage affirmative litigation or other steps to address that risk and increase Alphabet's resilience to risk. GSU grants are not guaranteed, are discretionary, are subject to approval by the Alphabet Inc. board of directors or its delegate, the terms of the relevant Alphabet Inc. stock plan, and your grant agreement.

4 days ago

Alameda, CA

The position oversees the surveillance, triage, interpretation, and dissemination of global regulatory intelligence across Research & Development (R&D), Quality (QA), Information Technology (IT) and Pharmaceutical Supply Chain (PSC), partnering with cross-functional subject matter experts to ensure impact assessments are conducted and documented.

EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:

Education:

BA/BA degree in related discipline and 15 years of related experience; or,
MA/MA degree in related discipline and 13 years of related experience; or,
PhD in related discipline and 12 years of related experience; or,
Equivalent combination of education and experience.

30+ days ago

Palo Alto, CA

$185,000–$205,000

li>Contributes to the development of global clinical and regulatory plans and strategies, identifies and proposes risk mitigation strategies, and influences project teams and sub teams across international site locations.

Do you want to be part of building a fully integrated biopharmaceutical company together with a team of highly skilled colleagues who are passionate about developing best-in-class therapeutics that address significant unmet medical needs?

30+ days ago

South San Francisco, CA

$235,000–$285,000 / year

p>Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. This individual will be responsible for developing and implementing regulatory plans and submissions to support preclinical and clinical development, IND/CTA submissions, and interactions with global health authorities.

21 days ago

San Diego, CA

$154,000–$193,000 / year

We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs.

The Associate Director, Regulatory Affairs Project Planning & Coordination is responsible for developing, implementing, and monitoring project plans and best practices that facilitate how the Global Regulatory Affairs department executes its strategic and functional goals.

30+ days ago

South San Francisco, CA

$170,000–$210,000 / 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.

30+ days ago

Redwood City, CA

$211,000–$264,000 / year

The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Required Skills, Experience and Education: Degree in life sciences, pharmacy, medicine, or related fields with a minimum of 15 years in the pharmaceutical/biotech industry or relevant work experience and a minimum of 8 years in Regulatory Affairs including regulatory strategy and leadership roles.

30+ days ago

Foster City, CA

$205,000–$225,000 / year

p>Education /Experience:

Bachelor's or advanced degree in a scientific discipline, with a minimum of 8 years in Regulatory Affairs with a minimum of 6 years of experience in the regulatory review of advertising and promotional materials for prescription drug and/or biologic products.
Manage and author commercial regulatory submissions, working closely with the Publishing vendor to ensure timely publishing and submission of promotional materials to the Office of Prescription Drug Promotion (OPDP).

30+ days ago

Sacramento, CA

We bring together a diverse, cross-sector network to prevent and end homelessness, increase the supply of safe, stable, affordable homes, and reverse the legacy of systemic racial and economic inequities by building power among the people most impacted by housing injustice in partnership with cross-sector partners, shaping the narrative, and advocating for the passage of transformative statewide policy solutions. The position is expected to participate in regular travel (mostly in California) including the following engagements: twice yearly Board of Directors meetings (sometimes held in Sacramento); annual 2-3 day staff retreat; annual 3-day Housing California conference (often in Sacramento); annual 2-3-day statewide RUN summit (sometimes in Sacramento); plus various conferences or in-person partner meetings, based on need and interest.

12 days ago

Redwood City, CA

$211,000–$264,000 / year

Required Skills, Experience and Education:

Degree in life sciences, pharmacy, medicine, or related fields with a minimum of 12 years in the pharmaceutical/biotech industry or relevant work experience and a minimum of 8 years in Regulatory Affairs including a regulatory strategy role.

30+ days ago

Redwood City, CA

$211,000–$264,000 / year

Required Skills, Experience and Education:

Degree in life sciences, pharmacy, medicine, or related fields with a minimum of 12 years in the pharmaceutical/biotech industry or relevant work experience and a minimum of 8 years in Regulatory Affairs including a regulatory strategy role.

30+ days ago

Redwood City, California

The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below.

30+ days ago

Redwood City, California

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below.

30+ days ago

San Diego, CA

$210,000–$230,000 / year

li>Manage development, review, approval, and version control of labeling documents, including Target Product Labeling, Core Labeling (e.g., Company Core Data Sheet [CCDS]), and Regional Labeling (e.g., USPI, EU SmPC), in a timely manner according to internal SOPs and external regulatory requirements. 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.

2 days ago

San Diego, CA

Remote

$240,000–$265,000

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The Senior Director of Regulatory Affairs leads global regulatory activities and manages personnel for IND/CTA preparations, meetings, and maintenance to support new and ongoing development programs. Contineum Therapeutics (Nasdaq: CTNM) is a clinical-stage biopharmaceutical company pioneering novel, oral small molecule therapies for NI&I indications with significant unmet need.

30+ days ago

$175,000–$219,000 / year

We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy.

30+ days ago

San Francisco, CA

$195,500–$272,500 / year

p>Vir Biotechnology is seeking an a highly motivated, self-driven and enthusiastic Director of Regulatory CMC accountable for ensuring all assigned products have a successful regulatory CMC strategy for clinical development and commercialization.

Manage CMC regulatory changes throughout the product life cycle, including support for relevant quality systems related to change control, discrepancy management, as well as Health Authority inspection support (as applicable).

2 days ago

Sunnyvale, CA

This role is a Director-level Regulatory Affairs leader, who will work with business unit leaders, clinical teams, reimbursement teams to define and execute global cardiac regulatory strategy, leads a cross-functional team leveraging regional teams and programs, ensures competitive market access, and represents the organization in senior regulatory and industry external facing activities.

Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process).

30+ days ago

San Carlos, CA

Remote

$170,000–$200,000 / year

ul>

Collaborates closely with functional leaders to 1) create the optimal development path for Iovance product candidates, 2) negotiate optimal development paths within cross-functional teams and with health authorities, 3) execute clinical-regulatory development plans on-time and while managing all identified risks.

Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to manage work-related stress; ability to manage multiple priorities simultaneously; and ability to meet deadlines.

4 days ago

Foster City, California

li>Manage and author commercial regulatory submissions, working closely with the Publishing vendor to ensure timely publishing and submission of promotional materials to the Office of Prescription Drug Promotion (OPDP).

Bachelor’s or advanced degree in a scientific discipline, with a minimum of 8 years in Regulatory Affairs with a minimum of 6 years of experience in the regulatory review of advertising and promotional materials for prescription drug and/or biologic products.

18 days ago

Redwood City, CA

$211,000–$264,000 / year

Required Skills, Experience and Education:

Degree in life sciences, pharmacy, medicine, or related fields with a minimum of 12 years in the pharmaceutical/biotech industry or relevant work experience and a minimum of 8 years in Regulatory Affairs including a regulatory strategy role.

30+ days ago

Redwood City, California

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below.

30+ days ago

Brisbane, CA

This role will be responsible for developing the global regulatory strategy in collaboration with key internal stakeholders, as well as tactical implementation of that strategy guiding and executing compliant, high quality, nonclinical and clinical submissions and interactions in support of early development, registration and life cycle management activities.

Works strategically with all regulatory functions to develop detailed, actionable submission plans, tracks major submission deliverables, and ensures consistent management submission documents, health authority communications, and all other regulatory information supporting Nurix's investigational and marketing applications.

30+ days ago

Brisbane, CA

The successful candidate will be a core member of the Regulatory team and will be responsible for helping build and execute on global regulatory strategy, objectives, policies and programs pertaining to development and future marketing of products for guiding and executing upon regulatory strategy of compliant, high quality, nonclinical and clinical submissions and interactions in support of early development, registration and life cycle management activities.

30+ days ago

Menlo Park, CA

$161,000–$187,000 / year

Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. This individual will work closely with cross-functional teams to provide regulatory guidance throughout product development, support health authority interactions, and help ensure the timely preparation and submission of high-quality regulatory applications.

22 days ago

San Diego, CA

$280,000–$320,000 / 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. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes.

30+ days ago

San Diego, California

This role requires a hands-on regulatory leader with deep experience in early clinical development (Phase 1/2), coordinating multiple parallel regulatory initiatives, strong health authority interaction experience, the ability to exercise judgment with decisions that have long-term impact on regulatory function success, and guide teams through ambiguity and evolving data. This individual will lead global regulatory strategy for one or more programs while influencing and partnering closely with cross-functional stakeholders to shape development plans and ensuring alignment across functions in a dynamic, fast-paced environment.

30+ days ago

Los Angeles, CA

$280,000–$320,000 / year

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California pay range

$280,000—$320,000 USD

Arrowhead provides competitive salaries and an excellent benefit package. 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.

21 days ago

Alameda, CA

$248,000–$352,500 / year

p>EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:

Education/Experience:

Bachelor's degree in related discipline and a minimum of fifteen years of related experience; or,
Master's degree in related discipline and a minimum of thirteen years of related experience; or,
PhD degree in related discipline and a minimum of twelve years of related experience; or,
Equivalent combination of education and experience.
Lead, author and evaluate documents submitted to regulatory health authorities to ensure they are complete, organized, of high quality, contain appropriate messaging and compliant with applicable regional regulations.

25 days ago

Alameda, CA

$195,000–$277,500 / year

EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: Bachelor's degree in related discipline and a minimum of eleven years of related experience; or, Master's degree in related discipline and a minimum of nine years of related experience; or, PhD degree in related discipline and a minimum of five years of related experience; or, Equivalent combination of education and experience. Experience/The Ideal for Successful Entry into Job: Knowledge/Skills: Develops and manages plans within established timelines and balances commitments to complete multiple activities and achieve results.

26 days ago

South San Francisco, CA

$218,058.40–$327,087.60 / year

Working with colleagues across locations, therapy areas and external partners, this role offers the chance to influence strategy end-to-end, from early development through rapid global approvals, while learning from leading experts, sharing best practices and using data, technology and modern approaches to reduce barriers for patients worldwide. 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.

30+ days ago

Redwood City, CA

$238,900–$281,100 / year

The pay range that the Company reasonably expects to pay for this headquarters-based position is $238,900 - $281,100; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today.

30+ days ago

Alameda, California

$133.33–$153.33 / hour

Bachelor's degree in related discipline and a minimum of thirteen years of related experience; or, · Master's degree in related discipline and a minimum of eleven years of related experience; or, · PhD degree in related discipline and a minimum of eight years of related experience; or, · Equivalent combination of education and experience. Leads the systematic collection, analysis, and dissemination of regulatory intelligence to proactively inform our client's policies, processes, and practices, enabling subject matter experts to assess the impact of evolving global regulatory requirements and translate regulatory changes into actionable guidance.

30+ days ago

Alameda, CA

$148,700–$297,300 / year

The individual will play a critical role in anticipating and influencing evolving regulations and guidance, lead complex management change initiatives, interface with outside regulatory agencies and trade associations, and advise executive management with strategic insights and key regulatory metrics. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.

30+ days ago

San Diego, CA

$228,000–$245,000 / year

p>The Director Global Regulatory Affairs will play a critical role in developing and implementing regulatory strategies to support the global development and expansion of Januxs clinical pipeline.

Proven track record of successful regulatory submissions and approvals alongside successful direct interaction with global regulatory agencies FDA EMA MHRA and others.

30+ days ago

Sunnyvale, CA

p>Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process). Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status.

30+ days ago

San Francisco, CA

$285,000–$320,000 / year

The ideal candidate brings deep Regulatory CMC expertise, strong cross-functional leadership skills, demonstrated experience with global and ROW filings (e.g., MENA, LATAM, APAC), and practical fluency leveraging AI-enabled and digital tools to improve regulatory workflows and deliverables.

Demonstrated experience leading complex global regulatory submissions, including Rest of World (ROW) regions (e.g., MENA, LATAM, APAC), with ability to navigate regional regulatory requirements and coordinate cross-regional filing strategies.

30+ days ago

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Director Of Regulatory Affairs Jobs in California

Sr Manager of Quality & Regulatory Michael Page USA

Director of Regulatory Affairs and Policy SupplyBank.org

Director of Regulatory Affairs Radiant Industries Inc

Executive Director of Regulatory Affairs - Obesity and Related Conditions Amgen Inc

Director of Regulatory Affairs Radiant Industries

Director of Regulatory Affairs Epia Neuro

Director of Regulatory Affairs The Scripps Research Institute

Director of Environmental Regulatory Affairs & Restoration Resource Environmental Solutions LLC

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

Senior Director, Head of Early Development Regulatory Affairs Revolution Medicines

Senior Director, Head of Early Development Regulatory Affairs Revolution Medicines Inc

Associate Director, Regulatory Affairs Global Regulatory Advertising and Promotion Arrowhead Pharmaceuticals Inc

Director, Regulatory Affairs Mapp Biopharmaceutical

Director, Regulatory Affairs, Global Investigations and Enforcement Competition Google LLC

Senior Director, Regulatory Affairs Policy, Regulatory Intelligence & Compliance Exelixis Inc

Associate Director, Global Regulatory Affairs Clinical Strategy - Job ID: 1961 Ascendis Pharma

Director/Senior Director, Regulatory Affairs Septerna

Associate Director, Regulatory Affairs Project Planning & Coordination Acadia Pharmaceuticals Inc

Associate Director, Regulatory Affairs Allogene Therapeutics Inc

Director, Regulatory Affairs Revolution Medicines Inc

Associate Director, Regulatory Affairs Advertising and Promotion Mirum Pharmaceuticals Inc

LEGISLATIVE AND REGULATORY AFFAIRS DIRECTOR AT HOUSING CALIFORNIA Axis Talent Partners

Director, Regulatory Affairs US Filing Lead Revolution Medicines Inc

Director, Regulatory Affairs - US Filing Lead Revolution Medicines Inc

Director, Regulatory Affairs (US Filing Lead) Revolution Medicines

Director, Regulatory Affairs - US Filing Lead Revolution Medicines

Director, Regulatory Affairs Labeling Arrowhead Pharmaceuticals Inc

Senior Director, Regulatory Affairs Contineum Therapeutics

Director, Regulatory Affairs Thermo Fisher Scientific Inc

Director, CMC Regulatory Affairs Vir Biotechnology Inc

Director Regulatory Affairs - Cardiac Intuitive Surgical Inc

Associate Director, Regulatory Affairs Iovance Biotherapeutics Inc

Associate Director, Regulatory Affairs Advertising and Promotion Mirum Pharmaceuticals

Director, Regulatory Affairs Global Filing Lead Revolution Medicines Inc

Director, Regulatory Affairs (Global Filing Lead) Revolution Medicines

Director, Regulatory Affairs Nurix Therapeutics Inc

Associate Director, Regulatory Affairs Strategy, Hematology Oncology Nurix Therapeutics Inc

Sr. Manager/Associate Director, Regulatory Affairs Oruka Therapeutics Inc

Executive Director, Regulatory Affairs Arrowhead Pharmaceuticals Inc

Senior Director, Global Regulatory Affairs Janux Therapeutics

Executive Director, Regulatory Affairs Arrowhead Pharmaceuticals

Senior Director, Regulatory Affairs (Oncology) Exelixis Inc

Associate Regulatory Affairs Strategy Director (Oncology) Exelixis Inc

Senior Regulatory Affairs Director - Oncology Cell & Gene Therapy AstraZeneca Plc

Director, Regulatory Affairs CMC Corcept Therapeutics Inc

Regulatory Affairs Strategy Director Roth Staffing Companies

Associate Director, Regulatory Affairs (on-site) Abbott Laboratories

Director Global Regulatory Affairs Janux Therapeutics Inc

Director Multiport Regulatory Affairs Intuitive Surgical Inc

Sr. Director, Regulatory Affairs BridgeBio Pharma Inc

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