333 Results for

Regulatory Manager Jobs in San Francisco, CA

Jobs

New!

Sunnyvale, CA6 days ago

$50–$60 Per 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.

New!

South San Francisco, CAToday

$120–$128.78 Per Hour

Example Duties and ResponsibilitiesPRC Leadership: Lead/chair PRCs and effectively collaborate with cross-functional internal groups and external advertising agencies; acting as the decision-maker for PRCs in the assigned therapeutic or business area. 4 or more years' previous experience leading large-scale, cross-functional project teams or other forums in design, development and implementation of policies, programs or projects with significant organizational impact strongly preferred.

New!

Sunnyvale, CAToday

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.

New!

Palo Alto, CAToday

Remote

$232,000–$348,000 Per Year

Primary responsibilities of the oncology pharmacology team include establishing efficacy in relevant disease models, demonstrating differentiation relative to relevant comparators, determining PK/PD/efficacy relationships, characterizing mechanisms of action, identifying predictive disease models, indications, and biomarkers, driving preclinical discovery, supporting research and development of Jazz products and drug candidates overall, and designing and executing studies that address clinically relevant priorities. The oncology pharmacology team cross-functional, including participation in matrix teams assigned to specific products that include but are not limited to Clinical Development, Bioanalytical, Toxicology, Clinical Pharmacology, Biomarkers Regulatory Affairs, and Project Management.

Alameda, California30+ days ago

Remote

$85–$93.68 Per 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.

San Carlos, CA28 days ago

Remote

$140,000–$160,000 Per Year

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

Organizational and planning skills; ability to influence and negotiate professionally at various levels within the project team and with external partners while maintaining positive working relationships.

Foster City, CA14 days ago

$137,000–$187,000 Per Year

The Policy and Regulatory Affairs at Zoox is a cross-functional organization responsible for advancing Zoox's public policy, regulatory, and political goals, including working with state regulatory agencies, legislators, executive branch, and policymakers. Exceptional project management and organizational skills, with experience successfully supporting the execution of multiple complex, cross-functional projects simultaneously.

New!

San Carlos, CA6 days ago

Remote

$140,000–$160,000 Per Year

Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines. Organizational and planning skills; ability to influence and negotiate professionally at various levels within the project team and with external partners while maintaining positive working relationships.

San Francisco, California9 days ago

Remote

$135,000–$150,000 Per Year

Jade’s pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Participate in the review of key clinical and nonclinical documents (protocols, IBs, CSRs, DSURs, etc.) to ensure alignment with regulatory obligations and relevant guidelines (ICH, FDA, EMA, ROW).

San Francisco, California9 days ago

Our lead product candidate, BHB-1893, is a next-generation oral small-molecule cardiac myosin inhibitor (CMI) being developed for the treatment of obstructive HCM (oHCM) and non-obstructive HCM (nHCM). Reporting into the Vice President of Regulatory Affairs, this individual will manage the CRO(s) responsible for preparing CTAs, as well as coordinate preparation of cross‑functional deliverables and manage health authority queries and responses.

Alameda, CA30+ days ago

$114,000–$228,000 Per Year

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.

New!

Alameda, California2 days ago

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.

Alameda, CA19 days ago

$130,700–$261,300 Per 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.

Alameda, California13 days ago

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. Maintains expert working knowledge of laws, regulations and enforcement decisions related to Quality Assurance (QA), manufacturing and Research & Development (R&D) issues that may impact company operations and decision making; communicates such knowledge to all internal stakeholders.

South San Francisco, CA22 days ago

$153,000–$175,000 Per Year

p>Position Overview:

Sutro has a unique capability that enables new molecular entities to be designed using a hybrid of synthetic and recombinant technologies to create best in class therapeutics in the oncology and auto-immune disease space. Sutro is advancing a robust early-stage pipeline of novel exatecan and dual-payload antibody drug conjugates (ADCs), coupled with high-value collaborations and industry partnerships, which validate its continuous product innovation.

South San Francisco, CA13 days ago

$60–$96 Per Hour

Support regulatory activities related to special regulatory designations, including Orphan Drug Designation (ODD), Fast Track, Breakthrough Therapy Designation (BTD), PRIME, and similar programs. Maintain complete and accurate regulatory archives and trackers, including monthly FDA submission records for all INDs and global health authority communications, and coordinate with partners to ensure archival completeness.

Redwood City, CA30+ days ago

$164,000–$205,000 Per 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. The Opportunity: The Senior Manager of Regulatory Affairs will provide project teams with regulatory advice, manage and coordinate various Regulatory Affairs activities within and between departments, and obtain and maintain National Health Authority approvals for investigational products.

New!

Redwood City, CAToday

$164,000–$205,000 Per 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. As part of the Regulatory Affairs function, the Senior Manager will work under supervision to provide strategic regulatory advice on advertising/promotion and medical materials to the US organization for assigned products in accordance with business goals and objectives, FDA regulations/guidances, pharma guidelines, and company policy.

Redwood City, CA30+ days ago

$164,000–$205,000 Per Year

As part of the Regulatory Affairs function, the Senior Manager will work under supervision to provide strategic regulatory advice on advertising/promotion and medical materials to the US organization for assigned products in accordance with business goals and objectives, FDA regulations/guidances, pharma guidelines, and company policy.

New!

Alameda, CAToday

$130,700–$261,300 Per Year

Palo Alto, CA30+ days ago

$162,000–$186,000 Per Year

p>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.

The Senior Manager, Regulatory Affairs owns and executes U.S. and international regulatory strategy for the company's Class II MRI devices and Class I accessory devices across the product lifecycle-from development through commercialization and post-market change management.

Los Altos, CA30+ days ago

Remote

$140,000

p style="margin-top:12pt;margin-bottom:12pt;padding-left:24px">You will:

Monitor and analyze state-level regulatory proceedings, legislation, and utility plans related to grid modernization, data analytics, demand-side management, energy efficiency, and customer experience.
You will:
- Serve as a regulatory subject-matter expert for internal teams, providing context and interpretation of regulatory developments across markets.

South San Francisco, CA30+ days ago

$165,000–$195,000 Per Year

p>EDUCATION/EXPERIENCE/SKILLS:

Bachelor's or advanced degree in scientific discipline, with a minimum of 5 years of experience working in drug development in the biopharmaceutical industry and at least 3 years of experience in Regulatory Affairs; immunology or rare disease/ orphan drug development experience desirable.
We are seeking an exceptionally motivated individual to provide leadership and support to global regulatory activities to achieve Alumis' strategic vision in obtaining worldwide approvals to market our products.

Foster City, CA13 days ago

The Policy and Regulatory Affairs at Zoox is a cross-functional organization responsible for advancing Zoox's public policy, regulatory, and political goals, including working with state regulatory agencies, legislators, executive branch, and policymakers. The Policy and Regulatory Affairs Manager will support Zoox’s state policy portfolio, providing important project management, public policy analysis, and help to implement Zoox’s state policy strategy.

San Francisco, CA30+ days ago

Remote

$127,000–$165,000 Per Year

Lead FDA submissions (510(k) or pre-submissions) with the team, including wearable devices, as well as artificial intelligence (AI) Software as a Medical Device (SaMD) products. There have been instances where individuals not associated with iRhythm have impersonated iRhythm employees pretending to be involved in the iRhythm recruiting process, or created postings for positions that do not exist.

CA30+ days ago

$106,000–$197,000 Per Year

You have 3-5 years experience with PhD degree, 5-7 with Masters degree and 6-8 years with Bachelor degree in the field of IVDs/Medical devices/Pharma/Biopharmaceutical with significant experiences in Regulatory Affairs or equivalent. You understand the structure, key roles and responsibilities of external customers/stakeholders and communicate timely and effectively the needs of external customers/stakeholders.

San Francisco, California30+ days ago

Remote

New!

San Mateo, CAToday

$157,590–$203,940 Per Year

p>Undergraduate or advanced degree in life sciences or related field with significant CMC, manufacturing, research, development, regulatory or related work experience in the biopharma or related industry with at least 8 years of experience with a BA/BS, or 6 years with an MA/MS/MBA, or 2 years with a PhD or PharmD.

Responsible for preparing and submitting complex regulatory documents which require interaction with departments outside of CMC Regulatory Affairs for investigational and commercial products, in line with ICH requirements, regional requirements, and scientific and company policies and procedures.

New!

Palo Alto, CAToday

$162,000–$186,000 Per Year

p>Hyperfine, Inc. 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 brainimaging system capable of providing imaging at multiple points of care in a healthcare facility.

The Senior Manager, Regulatory Affairs owns and executes U.S. and international regulatory strategy for the company's Class II MRI devices and Class I accessory devices across the product lifecycle—from development through commercialization and post-market change management.

New!

Brisbane, CAToday

Leveraging Nurix's extensive expertise in E3 ligases together with its proprietary DNA-encoded libraries, Nurix has built DELigase, an integrated discovery platform to identify and advance novel drug candidates targeting E3 ligases, a broad class of enzymes that can modulate proteins within the cell. Nurix's wholly owned pipeline comprises targeted protein degraders of Bruton's tyrosine kinase (BTK), a B-cell signaling protein, and an inhibitor of Casitas B-lineage lymphoma proto-oncogene-B (CBL-B), an E3 ligase that regulates T cell activation.

Santa Clara, CA30+ days ago

$114,000–$228,000 Per Year

The candidate will combine knowledge of scientific, regulatory, and business issues to enable products, including combination products, that are developed, manufactured or distributed to meet required legislation. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.

San Carlos, CA14 days ago

$183,000–$194,000 Per Year

p>Essential Functions:

Represent Regulatory Affairs in various internal cross-functional project teams, improvement initiatives and providing regulatory positions on various CMC related topics.
Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked.

Brisbane, CA30+ days ago

$140,000–$214,000 Per Year

Vera Therapeutics' lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis.

Vera Therapeutics' receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Vera Therapeutics and such organization and will be considered unsolicited and Vera Therapeutics will not be responsible for related fees.

New!

Alameda, California5 days ago

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.

San Carlos, California9 days ago

$183,000–$194,000 Per Year

Essential Functions: Represent Regulatory Affairs in various internal cross-functional project teams, improvement initiatives and providing regulatory positions on various CMC related topics. Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked.

CA22 days ago

p>As a Manager on the Regulatory Response Team, you will work closely with members of Global Affairs and act as a team lead for a team of project managers that partner with counsel, to coordinate how Google responds to inquiries and investigations by government and regulatory agencies worldwide. As a Program Manager at Google, you'll lead complex, multi-disciplinary projects from start to finish - working with stakeholders to plan requirements, manage project schedules, identify risks, and communicate clearly with cross-functional partners across the company.

San Francisco, California27 days ago

$103,000–$138,000 Per Year

p style="margin:0px">A key function of this role will be to identify, research, analyze, and synthesize the cross section of regulatory and wholesale market rules impacting Pattern’s existing and planned assets in WECC, MISO, ERCOT, SPP, PJM and other priority markets as needed. Importantly, the role will support the coordination with expert consultants and internal SMEs to clearly and regularly identify and lead Pattern’s engagement in regulatory and market design changes, develop Pattern’s positions and execute on strategies to achieve desired objectives.

PALO ALTO, CA26 days ago

$66.52–$88.14 Per Hour

As a Project Manager - Regulatory & Licensing, you'll manage the licensing and regulatory coordination for healthcare projects, partnering closely with internal medical planning and regulatory affairs teams, external design teams, and authorities having jurisdiction. The Design and Construction Project Manager is responsible for managing the day-to-day efforts related to programming, planning, design, construction, and activation of small projects for the Stanford Health Care (SHC) under the general supervision of the Director.

Palo Alto, CA30+ days ago

$186,000–$232,500 Per Year

Rivian may use your Candidate Personal Data for the purposes of (i) tracking interactions with our recruiting system; (ii) carrying out, analyzing and improving our application and recruitment process, including assessing you and your application and conducting employment, background and reference checks; (iii) establishing an employment relationship or entering into an employment contract with you; (iv) complying with our legal, regulatory and corporate governance obligations; (v) recordkeeping; (vi) ensuring network and information security and preventing fraud; and (vii) as otherwise required or permitted by applicable law. Rivian may share your Candidate Personal Data with (i) internal personnel who have a need to know such information in order to perform their duties, including individuals on our People Team, Finance, Legal, and the team(s) with the position(s) for which you are applying; (ii) Rivian affiliates; and (iii) Rivian's service providers, including providers of background checks, staffing services, and cloud services.

San Francisco, CA26 days ago

$103,000–$138,000 Per Year

p>A key function of this role will be to identify, research, analyze, and synthesize the cross section of regulatory and wholesale market rules impacting Pattern's existing and planned assets in WECC, MISO, ERCOT, SPP, PJM and other priority markets as needed. Importantly, the role will support the coordination with expert consultants and internal SMEs to clearly and regularly identify and lead Pattern's engagement in regulatory and market design changes, develop Pattern's positions and execute on strategies to achieve desired objectives.

Alameda, CA30+ days ago

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: HApWOKJEzq0IQxi15tNrlpXMJkFtE7qhBCo6PVler_t91rUjMytuOw.

Newark, CA30+ days ago

$117,000–$143,000 Per Year

This role will ensure regulatory information and documentation are maintained accurately and efficiently across systems that support regulatory submissions, health authority interactions, and product lifecycle management. The Regulatory Systems Manager will play a key role in improving processes, ensuring data integrity, supporting system implementations, configuration, or upgrades, and enabling efficient regulatory submissions and compliance.

San Francisco, CA16 days ago

$315,000–$385,000 Per Year

In addition to managing and developing the team, you will work directly with strategic customers, help shape Harvey's go-to-market approach, and partner cross-functionally with Product, Marketing, Enablement, and Engineering to improve how Harvey serves the legal industry.

Qualified lawyer with 7+ PQE, including significant experience practicing litigation, regulatory, investigations, compliance, white-collar defense, enforcement, employment litigation, financial regulatory matters, government investigations, or other contentious legal work, including experience working in-house.

San Francisco, California19 days ago

In addition to managing and developing the team, you will work directly with strategic customers, help shape Harvey’s go-to-market approach, and partner cross-functionally with Product, Marketing, Enablement, and Engineering to improve how Harvey serves the legal industry. Qualified lawyer with 7+ PQE, including significant experience practicing litigation, regulatory, investigations, compliance, white-collar defense, enforcement, employment litigation, financial regulatory matters, government investigations, or other contentious legal work, including experience working in-house.

New!

Palo Alto, California2 days ago

$173,000–$216,300 Per Year

ul style="margin-top: 0; margin-bottom: 0;">

Enabling Deployment: By developing credible, evidence-based safety cases supporting governmental approvals, you directly enable the commercialization and deployment of Rivian’s L3/4 autonomous systems on public roads..

Regulatory Trust: As a primary technical expert for regulators, you build the transparency and trust necessary for Rivian to navigate complex, evolving global approval processes..

CA25 days ago

As a Program Manager in the Regulatory PMO, you will work closely with members of Regulatory Affairs and act as the central project manager in partnership with counsel, to coordinate how Google responds to inquiries and investigations by government and regulatory agencies worldwide. As a Program Manager at Google, you'll lead complex, multi-disciplinary projects from start to finish - working with stakeholders to plan requirements, manage project schedules, identify risks, and communicate clearly with cross-functional partners across the company.

New!

Palo Alto, CA1 day ago

$173,000–$216,300 Per Year

CA25 days ago

p>As a Program Manager in the Regulatory PMO, you will work closely with members of Regulatory Affairs and act as the central project manager in partnership with counsel, to coordinate how Google responds to inquiries and investigations by government and regulatory agencies worldwide. As a Program Manager at Google, you'll lead complex, multi-disciplinary projects from start to finish - working with stakeholders to plan requirements, manage project schedules, identify risks, and communicate clearly with cross-functional partners across the company.

Oakland, CA25 days ago

$128,000–$252,200 Per Year

The position resides within the Strategic Regulatory group in the Legal & External Affairs function and serves as the enterprise lead for interpretation and assessment of EPR regulatory requirements that impact Clorox's products and packaging.

8+ years of relevant experience in regulatory affairs, product stewardship, compliance, or a related technical/regulatory function within consumer products, manufacturing, or another regulated industry.

Menlo Park, CA24 days ago

$161,000–$187,000 Per 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.

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Regulatory Manager Jobs in San Francisco, CA

Regulatory Affairs Specialist DGN Technologies Inc

Senior Program Director, Commercial Regulatory Affairs - Contract TalentBurst, Inc.

Sr. Regulatory Affairs - Contract TalentBurst, Inc.

Senior Director, Oncology Pharmacology Jazz Pharmaceuticals

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

Manager, Regulatory Affairs CMC Iovance Biotherapeutics Inc

Policy & Regulatory Affairs Manager Zoox Inc

Manager, Regulatory Affairs Iovance Biotherapeutics Inc

Manager, Regulatory Affairs Jade Biosciences

(Senior) Manager, Regulatory Affairs Braveheart Bio

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

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

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

Regulatory Affairs Manager - International Compliance Operations – Diabetes Care (on-site) Abbott

SENIOR MANAGER, REGULATORY AFFAIRS Sutro Biopharma Inc

Regulatory Affairs Manager Actalent Inc

Senior Manager, Regulatory Affairs Revolution Medicines Inc

Senior Manager, Commercial Regulatory Affairs Revolution Medicines

Senior Manager, Commercial Regulatory Affairs Revolution Medicines Inc

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

Senior Manager, Regulatory Affairs Hyperfine Inc

Manager, Regulatory Affairs & Market Development Bidgely Inc.

Senior Manager Regulatory Affairs contract Alumis Inc

Policy & Regulatory Affairs Manager Zoox

Manager, Regulatory Affairs iRhythm Holdings Inc

Regulatory Affairs Manager F. Hoffmann-La Roche Ltd

Manager, Regulatory Affairs iRhythm

Sr Manager, Regulatory Affairs CMC Gilead

Senior Manager, Regulatory Affairs Hyperfine | AI-Powered Portable MRI

Senior Manager, Regulatory Operations Nurix

Regulatory Affairs Manager - Vascular (on-site) Abbott Laboratories

Sr. Manager, Regulatory Affairs Vaxcyte Inc

Senior Manager, Regulatory CMC Vera Therapeutics Inc

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

Sr. Manager, Regulatory Affairs Vaxcyte

Manager, Regulatory Response Google LLC

Manager, Regulatory and Market Affairs Pattern Energy Group LP

Project Manager - Regulatory and Licensing Stanford Health Care

Manager, ADS Safety Case, Regulatory Rivian Automotive Inc

Manager, Regulatory and Market Affairs Pattern Energy Group Inc

Regulatory Affairs Manager - International Compliance Operations - Diabetes Care (on-site) Abbott Laboratories

Regulatory Systems Manager Ardelyx Inc

Legal Engineering Manager, In-House (Litigation/Regulatory) Counsel AI Corp

Legal Engineering Manager, In-House (Litigation/Regulatory) Harvey

Senior Manager, ADS Safety Case & Global Regulatory Strategy Rivian

Program Manager, Regulatory Program Management Office Google LLC

Senior Manager, ADS Safety Case & Global Regulatory Strategy Rivian Automotive Inc

Senior Program Manager, Regulatory Program Management Office Google LLC

Regulatory Senior Manager - EPR The Clorox Co

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

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