3,044 Results for

Regulatory Affairs Jobs in California

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Director Regulatory Affairs - CMC Clinical Dynamix, Inc.

San Diego, CA

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Responsible for the regulatory CMC leadership of one or more commercial and development projects, including responsibility for regulatory strategy, IND/CTA preparation, maintenance and update activities, interaction with and preparation for key milestone meetings with regulatory agencies with focus on the CMC aspects. Extensive project regulatory leadership and expertise, specifically focused on the CMC aspects for small molecules, biologics, and/or gene therapies.

5 days ago

Executive Director Regulatory Affairs Strategy Clinical Dynamix, Inc.

San Diego, CA

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The Executive Director will serve as a key voice at senior leadership tables, influencing cross-functional decisions to optimize regulatory pathways, accelerate development timelines, and enhance long-term commercial value. The Executive Director, Regulatory Strategy – Endocrinology is a senior regulatory leader responsible for shaping and driving global regulatory strategy across Company’s Endocrinology pipeline, spanning early development through commercialization.

5 days ago

Medical Affairs Associate # 26-27805 US Tech Solutions, Inc.

Santa Monica, CA

Remote

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The individual contributes to the operational execution of treatment-use and clinical support activities by coordinating study- and program-related deliverables, managing vendors and external partners, supporting site and investigator communications, tracking key milestones and risks, and helping ensure activities are conducted in alignment with applicable regulations, internal procedures, and program requirements. May assist in the review of study-related and essential start-up documents, as delegated by the study manager, including clinical protocols, informed consent forms, investigator brochures, pharmacy manuals, monitoring plans, case report forms, CRF completion guidelines, and other relevant study plans and charters.

7 days ago

Quality Systems & Regulatory Manager Jobot

Los Angeles, CA

$90,000–$120,000 / year
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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. They’re looking for a tech-savvy and detail-oriented Quality Systems & Regulatory Manager to lead food safety systems, labeling accuracy, customer compliance documentation, and cross-functional audit readiness.

9 days ago

Compliance & Regulatory Specialist, Consumer Packaged Goods System One

Ontario, CA

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System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. Requirements Bachelor's degree in Quality Assurance, Regulatory Affairs, Engineering, or a related field.

10 days ago

Compliance Regulatory Analyst Axelon

Oakland, CA

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Partner with cross-functional teams, including Operations, Engineering, Law, and Regulatory Affairs, to gather information, provide compliance support, and assist with implementation activities. Maintain compliance documentation, guidance materials, requirement inventories, and tracking tools to support implementation, audits, investigations, and regulatory inquiries.

6 days ago

Technical Regulatory Documentation Specialist System One

South San Francisco, CA

$45–$50 / hour
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Manage collaborations by coordinating document hand-offs and review cycles between subject matter experts, authors, publishing teams, and stakeholders in Development Sciences, Regulatory Affairs, and other functions. Provide essential support for document lifecycle management, data entry, and workflow coordination for nonclinical documents supporting various regulatory submission types.

3 days ago

Manager, Accreditation & Regulatory Compliance (White Memorial) Adventist Health

Los Angeles, CA

Job Summary: Directs day-to-day regulatory readiness activities, including internal audits, mock surveys, tracer programs, and regulatory education across clinical and operational departments at assigned hospitals/markets. Leads site/network accreditation, regulatory compliance, and licensing operations, ensuring continuous readiness and alignment with Centers for Medicare & Medicaid Services (CMS), The Joint Commission, and state requirements.

30+ days ago

Associate Director* Genesis10

Temporary
Contractor
Full time
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Responsibilities: Provide accurate, balanced, evidence-based, and timely responses to unsolicited medical and scientific inquiries from healthcare professionals, patients or caregivers, and internal colleagues, using approved response documents, current literature, and appropriate data on file. A key focus of the role will be supporting Medical Information readiness for the upcoming multiple myeloma launch, including development of scientific response resources, management of anticipated inquiry topics, and preparation of internal and external support teams.

12 days ago

Senior Director, Content Studio & Digital Operations # 26-27466 US Tech Solutions, Inc.

South San Francisco, CA

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In this role, you will define the business and operational strategy to elevate customer engagement, establish lead and further a tech-enabled service organization to deliver exceptional quality, accelerate production cycles, and optimize end-to-end operations for maximum efficiency and cost savings. As healthcare evolves, we are leading with bold initiatives—leveraging cutting-edge AI, advanced digital engagement model, end-to-end content management, and omnichannel operations to create seamless, personalized, and meaningful experiences.

11 days ago

Senior Director, Global Medical Director, Breast Cancer Jazz Pharmaceuticals

Palo Alto, CA

Remote

$268,000–$402,000 / year

The role serves as a critical interface between regional Medical Affairs teams and global R&D, Global Product Development and Commercialization functions, partnering closely with US and EUR/INT colleagues to ensure regional insights and priorities are understood, communicated, and appropriately considered within the Clinical Development Team (CDT), Late Development Team (LDT), Medical Functional Matrix Team (mFMT), and governance forums including the Product Governance Committee (PGC) and Development Project Review Committee (DPRC). Success in this role requires strong partnership with regional teams, particularly in the US, to maintain close alignment with regional medical strategies and ensure that evidence generation activities and development plans address the needs of physicians, patients, and healthcare systems across regions.

1 day ago

Regulatory Affairs Specialist, Regulatory Intelligence & Corporate Regulatory Affairs Edwards Lifesciences Corp

Irvine, CA

$74,000–$104,000 / year

What You'll Need (Required): Bachelor's degree and minimum of (3) three years of Regulatory Affairs experience within a highly regulated industry OR Master's degree with at least (1) one year of Regulatory Affairs experience within a highly regulated industry; or equivalent work experience based on Edwards' criteria. How you will make an impact: Support the implementation of various Regulatory process improvement projects by working directly with key stakeholders in all business units as well as Edwards' international counterparts to accelerate market access routes and ensure compliance.

28 days ago

Product Complaints Coordinator Step Up Recruiting

Northridge, CA

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This position requires a strong understanding of quality management systems, excellent communication skills, and the ability to work collaboratively across departments to ensure timely resolution of complaints and implementation of corrective actions. Conduct thorough investigations into each complaint, gathering relevant information from internal sources (e.g., production/batch records, quality control data) and external sources (e.g., customer feedback, returned products).

5 days ago

Assembler 22nd Century Technologies Inc. (TSCTI)

Irvine, CA

As one of the nation's leading Healthcare Workforce Solutions providers, TSCTI supports federal healthcare systems, Veterans Affairs (VA) Medical Centers, state and local healthcare agencies, hospitals, clinics, laboratories, long-term care facilities, and commercial healthcare organizations. Headquartered in Princeton, NJ, and McLean, VA, with 14 regional offices nationwide, TSCTI provides comprehensive solutions in Digital Transformation, Artificial Intelligence (AI), Cybersecurity, Cloud Computing, IT Infrastructure, Enterprise Modernization, DevSecOps, Managed Services, Workforce Solutions, and Healthcare Staffing.

Today

Regulatory Affairs Associate Akkodis Group AG.

Santa Clara, CA

$40–$45 / hour

The ideal candidate will develop and manage regulatory-compliant medical device labeling, including IFUs, product labels, and country-specific addendums while coordinating cross-functional stakeholders to ensure timely implementation. Regulatory Affairs Associate Responsibilities include: Develop, review, and maintain medical device labeling, including IFUs, product labels, import labels, and country-specific addendums.

8 days ago

Vice President, Medical Affairs, Clinical Operations & Regulatory Affairs Dendreon Pharmaceuticals

Seal Beach, California

With Immunotherapy Manufacturing Facilities in Seal Beach, CA, and Union City, GA, a talented team of scientific, clinical, regulatory, and corporate professionals based in Seal Beach, and a commercial organization operating across the United States, Dendreon continues to advance innovation in personalized cancer treatment. Develop and maintain strategic relationships with physicians, investigators, Key Opinion Leaders (KOLs), healthcare providers, and scientific experts to support clinical development, evidence generation, product adoption, and medical education initiatives.

Today

Regulatory Affairs Manager - US Regulatory Lead, Rare Disease Amgen Inc

Thousand Oaks, CA

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: A 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.

4 days ago

Regulatory Affairs Associate Actalent Inc

Santa Clara, CA

$40–$43 / hour

You will regularly use systems such as SAP MD, other SAP-based tools, Microsoft Office, and content management platforms like Adobe Acrobat Pro to manage labeling, documentation, and project activities. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

11 days ago

Regulatory Affairs Associate Select Source International

California, CA

Initiatives include but are not limited to: Label Design and Development: Collaborate with Regulatory Affairs specialists, international regulatory affiliates, and labeling project management to develop labeling strategies. The position will be responsible for designing, developing, and implementing international addendum labeling (IFUs, import labels, country-specific labeling) that meets international requirements for our medical devices.

9 days ago

Associate Director/ Director, Regulatory Affairs (Global Regulatory Advertising and Promotion) Arrowhead Pharmaceuticals

Los Angeles, CA

$180,000–$240,000 / year

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.

30+ days ago

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Regulatory Affairs Jobs in California

Director Regulatory Affairs - CMC Clinical Dynamix, Inc.

Executive Director Regulatory Affairs Strategy Clinical Dynamix, Inc.

Medical Affairs Associate # 26-27805 US Tech Solutions, Inc.

Quality Systems & Regulatory Manager Jobot

Compliance & Regulatory Specialist, Consumer Packaged Goods System One

Compliance Regulatory Analyst Axelon

Technical Regulatory Documentation Specialist System One

Manager, Accreditation & Regulatory Compliance (White Memorial) Adventist Health

Associate Director* Genesis10

Senior Director, Content Studio & Digital Operations # 26-27466 US Tech Solutions, Inc.

Senior Director, Global Medical Director, Breast Cancer Jazz Pharmaceuticals

Regulatory Affairs Specialist, Regulatory Intelligence & Corporate Regulatory Affairs Edwards Lifesciences Corp

Product Complaints Coordinator Step Up Recruiting

Assembler 22nd Century Technologies Inc. (TSCTI)

Regulatory Affairs Associate Akkodis Group AG.

Vice President, Medical Affairs, Clinical Operations & Regulatory Affairs Dendreon Pharmaceuticals

Regulatory Affairs Manager - US Regulatory Lead, Rare Disease Amgen Inc

Regulatory Affairs Associate Actalent Inc

Regulatory Affairs Associate Select Source International

Associate Director/ Director, Regulatory Affairs (Global Regulatory Advertising and Promotion) Arrowhead Pharmaceuticals

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