1,007 Results for

Regulatory Specialist Jobs in San Francisco, CA

Jobs

Sunnyvale, CA

$50–$60 / hour
Contractor

p tabindex="0">• Strong verbal and written communication skills, proven ability to translate technical documentation into effective internal documentation, and regulatory submissions.

• Provide regulatory guidance to product teams, develop regulatory plans, and review and approve product design control documentation.

5 days ago

Walnut, CA

$75,000–$105,000 / year

The team is looking for candidates who are skilled in conducting safety training, hazard analysis, incident investigations, hazardous waste management, environmental reporting, and maintaining compliance documentation, including SDS records, permits, and prevention plans. 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.

8 days ago

Emeryville, CA

$105,000–$120,000 / year

The firm provides innovative solutions across diverse markets, supporting technically complex projects that require regulatory rigor, cost control, schedule discipline, and creative structural design. 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.

8 days ago

Dublin, CA

$100,000–$150,000 / year

p>We are partnering with a growing, innovative medical device organization seeking a Senior Regulatory Affairs Specialist to support global regulatory strategy, submissions, and product lifecycle activities.

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.lhh.com/us/en/candidate-privacy.

30+ days ago

Alameda, CA

$100,000–$200,000 / year

li>Coordinate with cross functional teams including but not limited to: global Regulatory Affairs (e.g., APAC, CALA, EMEAP and US), Commercial, Marketing / PLC, Supply Planning, Customer Service, Quality, R&D, Operations, etc. to ensure all internal and external requirements are met prior to product release.

This Principal Regulatory Affairs Specialist position is responsible for leading strategic planning as well as developing and deploying innovative solutions to ensure timely regulatory registration and release of products for distribution into specific geographies in the growing Asia Pacific (APAC) market.

30+ days ago

Sunnyvale, CA

$53.65–$58.65 / hour

strong>Why Should You Apply?

6 days ago

Mountain View, CA

$56–$60

Minimum 8 years of Regulatory Affairs experience within a medical device company (experience may be combined with a Regulatory Affairs Master's degree, such as a Master's in Regulatory Science). Coordinate with technical experts to provide additional data and information requested by regulatory agencies and prepare responses to facilitate regulatory approvals.

4 days ago

Pleasanton, California

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Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree .

• Supports all business segment initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements .

30+ days ago

Sunnyvale, CA

$58–$59 / hour

Strong verbal and written communication skills, proven ability to translate technical documentation into effective internal documentation, and regulatory submissions. " Provide regulatory guidance to product teams, develop regulatory plans, and review and approve product design control documentation.

6 days ago

Alameda, California

li>Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.

28 days ago

Alameda, CA

$90,000–$180,000 / year

In this role, you will provide regulatory input on design and development activities to cross-functional teams, including software development and systems engineering members, and ensure availability of documentation to support submission activities to meet program objectives and timelines.

Represent Regulatory Affairs on cross functional project teams and provide strategic input and technical guidance on product lifecycle planning and regulatory requirements for Class II software medical devices.

18 days ago

Santa Clara, CA

$55–$59 / hour

p>Build your future with VoltVolt is immediately hiring for Senior Regulatory Affairs Specialist in Santa Clara CaliforniaAs a Senior Regulatory Affairs Specialistyou will Develops and implements programs and processes to ensure that company products are safe legal and meet or exceed customer expectations for compliance with nationalregionalglobal regulations. PAY RANGE AND BENEFITSPay Range 55 - 59 per hourPay range offered to a successful candidate will be based on several factors including the candidates education work experience work location specific job duties certifications etc.

13 days ago

Sunnyvale, CA

$53.65–$58.65 / hour

strong>Why Should You Apply?

5 days ago

Redwood City, CA

Pulmonx is a global leader in interventional pulmonology, providing minimally invasive technologies, planning tools, and evidence-based treatments for people living with severe emphysema and advanced chronic obstructive pulmonary disease (COPD), a progressive lung condition characterized by severe breathing difficulty that can significantly restrict daily activities and negatively impact quality of life. Manage the full lifecycle of domestic and international registrations across multiple products simultaneously, including Q-Subs, PMA modules/supplements, 510(k)s, IDEs, license renewals, and reportable changes; maintain global registration tracking for license status, expiration dates, and compliance obligations across all markets.

30+ days ago

Alameda, CA

$140,000–$185,000 / year

This role will drive global regulatory strategies for our medical device and biologic products, guide cross-functional teams through complex regulatory pathways, and ensure our innovative technology reaches patients safely and efficiently.

Spearhead rapid response efforts to regulatory agency communications, including deficiency letters, requests for additional information, and pre-submission feedback; drafting clear, persuasive responses while managing tight turnaround time.

30+ days ago

San Francisco, 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

Alameda, California

li>Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.

20 days ago

Palo Alto, CA

$145,000–$167,000 / year

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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.
Ensure regulatory submissions are authored according to applicable requirements and guidelines (as assigned) including, but not limited to:
- US FDA 510(k) submissions.

22 days ago

Sunnyvale, CA

30+ days ago

Sunnyvale, CA

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). U.S. 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

Sunnyvale, CA

Remote

$115,500–$156,400 / year

li>Reviews and approves document change orders, advertising and promotional material, technical documents, test protocols and reports, risk management documents, labeling documents, and other documents as a key member of assigned project teams and ongoing sustaining support.

Visit us at https://www.ebrsystemsinc.com/ to learn more-and join us in our work Empowering Physicians, Powering Hearts.

30+ days ago

Stanford, CA

Remote

$74,082–$143,544 / year

The Cardinal at Work website (https://cardinalatwork.stanford.edu/benefits-rewards) provides detailed information on Stanford's extensive range of benefits and rewards offered to employees.

Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University''s Administrative Guide, http://adminguide.stanford.edu.

30+ days ago

Santa Clara, CA

Remote

$43.80–$52.57 / hour

li> Proactively manages the changing regulatory environment for company products, prevents barriers to trade, eliminates duplication of effort and identifies and mitigates areas of risk.

Develops and implements programs and processes to ensure that company products are safe, legal and meet or exceed customer expectations for compliance with national/regional/global regulations.

1 day ago

Alameda, CA

$100,000–$200,000 / year

This is an exciting opportunity with responsibilities for leading global regulatory submissions, which include but not limited to premarket submissions, pre-submissions and clinical trial applications, which include medical hardware and digital health technology solutions to address the spectrum of customer needs. Apply Now Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life.

30+ days ago

Alameda, California

li>Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.

29 days ago

Alameda, CA

$100,000–$200,000 / year

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. The individual may monitor and influence changing regulations and guidance, interface with outside regulatory agencies and trade associations, develop innovative regulatory submission strategy, and provide executive management with regulatory metrics/information.

30+ days ago

Sunnyvale, CA

30+ days ago

Walnut Creek, CA

$104,236–$156,352 / year

p>As the largest global pure play sustainability consultancy, we partner with the world's leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations. Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safety, risk and social issues.

30+ days ago

Pleasanton, CA

$160,000–$175,000 / year

As a senior member of the Calyxo Regulatory Team, you will work closely with Research & Development, Operations, Quality, Clinical and Medical Affairs, Marketing, and Legal to ensure regulatory alignment from concept through commercialization—balancing speed with compliance as we bring category-defining medical devices to market.

Lead the strategy, preparation, submission, and negotiation of complex U.S. and international regulatory filings (including 510(k)s, Q-Subs/Pre-Submissions, Special 510(k)s, and Letters to File), ensuring timely approvals and serving as the technical lead on the most challenging submissions.

22 days ago

San Francisco, CA

p>The UCSF Memory and Aging Center (MAC) is an internationally renowned clinical and translational research center with over 300 full time employees with offices and clinical research space located in the Sandler Neurosciences Building and multiple other buildings on the UCSF Mission Bay Campus. The regulatory specialist collaborates closely with principal investigators, study teams, study sponsors, and administrative offices to facilitate timely study activation and maintain ongoing regulatory compliance in a complex academic research environment.

29 days ago

Walnut Creek, California

$111,000–$160,905 / year

p>As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations. Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safety, risk and social issues.

5 days ago

Walnut Creek, California

$93,050–$124,245 / year

5 days ago

Santa Clara, CA

p>If you provide content to customers through CloudFront, you can find steps to troubleshoot and help prevent this error by reviewing the CloudFront documentation.

Generated by cloudfront CloudFront Request ID: TwCqpv6BvTS-vlIXPJgAp7ukNfx9zn63Emu1GvSBFUGz6uk2CLaUZw.

30+ days ago

Sunnyvale, CA

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Acts as a regulatory representative on core product development teams, communicates regulatory requirements and impact of regulations to project teams, and provides input related to FDA and international product registrations and licensing requirements.

The Quality & Lean, Medical Devices Operational Compliance Center (MD-OCC), consists of business process analysts, quality system experts, program managers, supply chain experts, regulatory experts, clinical affairs, and internal auditors.

17 days ago

Alameda, California

li>Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.

12 days ago

Sunnyvale, CA

U.S. 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. 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 Ramon, California

$77,000–$115,000

div>Job Title: Regulatory Compliance Specialist

Organization: The Surplus Line Association of California (SLA)

Location: San Ramon, CA

Position Type: Full-time, Hybrid

Salary: $77,000 - $115,000

Position Overview:

The Surplus Line Association of California is seeking a Regulatory Compliance Specialist to support our members, strengthen compliance resources, and help advance understanding of California surplus line insurance requirements.

13 days ago

You will also partner with teams across Google and Alphabet's Public Policy, Compliance, Legal, Engineering, Finance and product areas to support the handling of some of the most important issues for the company today.

In this role, you will work closely with members of Regulatory Affairs and act as the central operations support for the department"s role in the broader regulatory lifecycle.

24 days ago

San Francisco, CA

$86,000–$112,000 / year

Business Development Specialist - Regulatory Marketing Department Summary We are seeking a results -oriented Business Development BD" Specialist to support the firms regulatory groups in marketing and developing new business. Reporting to the teams Assistant Director and managers for these groups the BD Specialist will deve lop knowledge and understanding of these practices and lawyers as well as the resources across the Marketing Department to collaborate on projects that secure new clients strengthen existing relationships and increase visibility of the practices.

30+ days ago

Alameda, CA

$114,000–$228,000 / year

You will be responsible for managing a small team overseeing the Diabetes Care product portfolio in the APAC region, creating robust global regulatory strategies, working with cross-functional teams as the regulatory SME, provide support for compiling regulatory submissions, and ensuring data is effectively presented for the registration of products in the APAC region.

This Regulatory Affairs Manager - APAC position will work closely with in-country regulatory representatives in the Asia Pacific (APAC) region to ensure efficient and compliant business processes and environment.

30+ days ago

Alameda, California

li>Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. You will be responsible for managing a small team overseeing the Diabetes Care product portfolio in the APAC region, creating robust global regulatory strategies, working with cross-functional teams as the regulatory SME, provide support for compiling regulatory submissions, and ensuring data is effectively presented for the registration of products in the APAC region.

28 days ago

San Francisco, California

Remote

$80–$120 / hour

li>Highly proficient in Microsoft Office and Google Workspace, especially Slides.

Work independently and asynchronously to meet deadlines and improve AI model performance.

19 days ago

Richmond, CA

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 .

30+ days ago

Alameda, CA

If you provide content to customers through CloudFront you can find steps to troubleshoot and help prevent this error by reviewing the CloudFront documentation. Generated by cloudfront CloudFront Request ID oQMSmMdag93U0tF6JuaDNwDM9MkzpH82GljciImZq5mNr9AKPKBXKQ.

30+ days ago

Alameda, CA

$130,700–$261,300 / year

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. Working on Lingo, you will help build a next-generation technology that enables individuals to make decisions about how to improve energy, lose weight or enhance athletic performance.

18 days ago

Alameda, California

li>Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.

6 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

San Mateo, CA

$340,000–$370,000 / year

This role will serve as the primary liaison with global regulatory authorities and involve close collaboration with Sagimets cross-functional teams and external partners, to ensure the successful advancement of our clinical programs.

Oversee the companys external regulatory advisors, consultants and vendors to ensure that relevant regulatory advice is provided with respect to the companys development programs.

30+ days ago

Alameda, California

Remote

$85–$93.68 / hour

Collaborate with Quality Assurance and cross‑functional stakeholders to support health authority inspections across GPS and Regulatory Affairs, ensuring the RA function remains in a continuous state of inspection readiness. · Work with Regulatory Affairs Strategist, CRO and Clinical Operations to ensure the Trial Master File (TMF) and Veeva RIM is kept current and complete for Regulatory Affairs-related documents.

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

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Regulatory Specialist Jobs in San Francisco, CA

Regulatory Affairs Specialist DGN Technologies Inc

EHS Specialist Jobot

Senior BIM Specialist Jobot

Senior Regulatory Affairs Specialist Lee Hecht Harrison

Principal Regulatory Affairs Specialist - APAC - Diabetes Care (on-site) Abbott Laboratories

Regulatory Affairs Specialist 4 ICONMA, LLC

Regulatory Affairs Specialist 4 - Mountain View, CA 94043 Amicis Global

Senior Regulatory Specialist Abbott

Regulatory Affairs Specialist 4 eTeam Inc.

Principal Regulatory Affairs Specialist – APAC - Diabetes Care (on-site) Abbott

Senior Regulatory Affairs Specialist - Lingo (on-site) Abbott Laboratories

Senior Regulatory Affairs Specialist Volt Information Sciences Inc

Regulatory Affairs Specialist 4 Iconma

Principal Regulatory Affairs Specialist Pulmonx Corp

Regulatory Specialist Science Corp

Regulatory Affairs Specialist 3 - Multiport da Vinci Intuitive Surgical Inc

Senior Regulatory Affairs Specialist – Lingo (on-site) Abbott

Senior Regulatory Affairs Specialist Hyperfine

Regulatory Affairs Specialist (NMPA) Intuitive Surgical Inc

Senior Regulatory Affairs Specialist Intuitive Surgical Inc

Senior Regulatory Affairs Specialist (Onsite/Remote) EBR Systems Inc

Cancer Clinical Trials Regulatory Specialist 2 (Remote) Stanford University

Senior Regulatory Affairs Specialist LanceSoft Inc

Principal Regulatory Affairs Specialist - Diabetes Care (on-site) Abbott Laboratories

Principal Regulatory Affairs Specialist - Diabetes Care (on-site) Abbott

Principle Regulatory Affairs Specialist - Diabetes Care (on-site) Abbott Laboratories

Regulatory Affairs Specialist 3 Intuitive Surgical Inc

Principal Consultant, Biologist/Regulatory Specialist, Power and Renewables ERM International Group Ltd

Staff Regulatory Affairs Specialist - Pleasanton, CA Calyxo

Regulatory Specialist UCSF Medical Center

Principal Consultant, Biologist/Regulatory Specialist, Power and Renewables ERM

Managing Technical Consultant, Permitting & Regulatory Specialist (Energy/Power/Renewable Projects) - California ERM

Senior Regulatory Affairs Specialist - Vascular (on-site) Abbott Laboratories

Sr. Regulatory Affairs Specialist , Medical Devices Operational Compliance Center (MD-OCC) Amazon.com Inc

Principal International Regulatory Product Specialist - Diabetes Care (on-site) Abbott

Regulatory Intelligence Specialist Intuitive Surgical Inc

Regulatory Compliance Specialist The Surplus Line Association of California

Strategy and Operations Lead, Regulatory Affairs Google LLC

Business Development Specialist- Regulatory Covington & Burling LLP

Regulatory Affairs Manager - APAC - Diabetes Care (on-site) Abbott Laboratories

Regulatory Affairs Manager – APAC - Diabetes Care (on-site) Abbott

Regulatory Compliance Specialist - Remote Mercor

Regulatory Affairs Coordinator Public Health Foundation Enterprises, In

Principal International Regulatory Product Specialist - Diabetes Care (on-site) Abbott Laboratories

Senior Manager, Regulatory Affairs - Lingo (on-site) Abbott Laboratories

Senior Manager, Regulatory Affairs - Lingo (on-site) Abbott

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

Vice President, Regulatory and Head of Regulatory Affairs Sagimet Biosciences Inc

Regulatory Affairs Quality/Standards/Training Manager - Remote Roth Staffing Companies

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

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