330 Results for

Regulatory Manager Jobs in Sunnyvale, CA

Jobs

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.

Foster City, CA14 days ago

$137,000–$187,000 Per Year

p>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.

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.

Alameda, CA30+ days ago

$114,000–$228,000 Per 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.

Alameda, California29 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. 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.

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

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.

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.

New!

San Carlos, CA6 days ago

Remote

$140,000–$160,000 Per Year

San Francisco, California9 days ago

Remote

$135,000–$150,000 Per Year

For more information, visit JadeBiosciences.com and follow the Company on LinkedIn.  . 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.

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.

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.

Redwood City, California30+ days ago

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.

Alameda, California7 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.

South San Francisco, CA13 days ago

$60–$96 Per Hour

li>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.

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.

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.

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.

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.

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.

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.

San Francisco, CA30+ days ago

Remote

$127,000–$165,000 Per Year

For more information, see https://www.ftc.gov/business-guidance/blog/2023/01/taking-ploy-out-employment-scams and https://www.ic3.gov/Media/Y2020/PSA200121.

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.

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.

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, California30+ days ago

Remote

p/>

For more information, see https://www.ftc.gov/business-guidance/blog/2023/01/taking-ploy-out-employment-scams and https://www.ic3.gov/Media/Y2020/PSA200121. Remote - US

Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.

CA30+ days ago

$106,000–$197,000 Per Year

li>

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.

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.

CA25 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.

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, 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.

San Carlos, California9 days ago

$183,000–$194,000 Per Year

div>

*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.

*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.

*MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.

Summary:.
Reports to: Executive Director, Regulatory CMC

Location: US - Remote

Work Arrangement (may be adjusted based on business needs, job responsibilities, or changes to company policy):
Remote

Compensation:
The compensation package will be competitive and includes comprehensive benefits and an equity component.

Salary Range: $183,000 - $194,000 (SF Bay Area).

New!

Oakland, CA3 days ago

$115,000–$130,000 Per 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.

New!

South San Francisco, CA1 day ago

$73.32–$179 Per Hour

This position leads Program Review Committees (PRCs), develops regulatory strategies, partners with cross-functional business leaders, and serves as the primary regulatory decision-maker supporting pharmaceutical advertising, promotion, product launches, and FDA communications.

This role supports the U.S. Commercial Regulatory Affairs organization and works across therapeutic areas and product portfolios to ensure promotional materials and regulatory submissions comply with FDA regulations, healthcare compliance requirements, and company policies.

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.

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!

Mountain View, CA6 days ago

li>

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.

Brisbane, CA30+ days ago

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.

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.

Brisbane, CA30+ days ago

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.

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.

New!

South San Francisco, CA1 day ago

Commercial Regulatory Affairs (CORA) is part that interprets the needs of worldwide health authorities and provides regulatory intelligence necessary to generate and present information that meets the needs of health authorities, patients, purchasers and prescribers for client s global Pharma Division, which includes all therapeutic areas and all phases of product development from early development to post marketing. " Must demonstrate in-depth knowledge of the bio/pharma industry (compliance, legal, clinical affairs, regulatory and product marketing) as well as in-depth knowledge of the legal and regulatory environment, as it relates to healthcare compliance in the bio/pharma industry (includes anti-kickback statutes, government fraud & abuse, off-label promotion, PhRMA Code, etc.).

New!

South San Francisco, CA1 day ago

Program Directors in CORA chair Program Review Committees (PRCs) for their assigned responsibilities, e.g., products within a designated therapeutic area(s) or cross-portfolio activities, such as managed care, interactive marketing, etc. Program Directors lead and manage the assigned PRCs and their activities; providing strategic and operational leadership in the areas of advertising and promotion regulatory review and approval for Roche pharmaceutical products.

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.

San Francisco, CA30+ days ago

$154,000–$193,000 Per 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.

Sunnyvale, CA30+ days ago

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).

New!

South San Francisco, CA1 day ago

$47.37–$127.86 Per Hour

strong> Responsibilities : Commercial Regulatory Affairs (CORA) is part that interprets the needs of worldwide health authorities and provides regulatory intelligence necessary to generate and present information that meets the needs of health authorities, patients, purchasers and prescribers for the firm's global Pharma Division, which includes all therapeutic areas and all phases of product development from early development to post marketing.

Must demonstrate in-depth knowledge of the bio/pharma industry (compliance, legal, clinical affairs, regulatory and product marketing) as well as in-depth knowledge of the legal and regulatory environment, as it relates to healthcare compliance in the bio/pharma industry (includes anti-kickback statutes, government fraud & abuse, off-label promotion, PhRMA Code, etc.).

New!

South San Francisco, CA1 day ago

$120–$128.78 Per Hour

strong> Example Duties and Responsibilities

PRC 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.

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.

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.

Palo Alto, CA30+ days ago

$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?

New!

South San Francisco, CA1 day ago

$50.56–$123.45 Per Hour

Our client is seeking an experienced Senior Program Director, Commercial Regulatory Affairs (CORA) to provide strategic and operational leadership supporting U.S. commercial regulatory activities. Commercial Regulatory Affairs serves as a key partner across Roche’s global pharmaceutical organization, providing regulatory expertise that supports product development through post-market activities.

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Regulatory Manager Jobs in Sunnyvale, CA

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

Policy & Regulatory Affairs Manager Zoox Inc

Manager, Regulatory Affairs CMC Iovance Biotherapeutics Inc

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

Manager, Regulatory Affairs Iovance Biotherapeutics Inc

Manager, Regulatory Affairs Jade Biosciences

Senior Manager, Regulatory Affairs Revolution Medicines Inc

Senior Manager, Commercial Regulatory Affairs Revolution Medicines Inc

Senior Manager, Commercial Regulatory Affairs Revolution Medicines

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

Regulatory Affairs Manager Actalent Inc

SENIOR MANAGER, REGULATORY AFFAIRS Sutro Biopharma Inc

(Senior) Manager, Regulatory Affairs Braveheart Bio

Sr Manager, Regulatory Affairs CMC Gilead

Senior Manager, Regulatory Affairs Hyperfine Inc

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

Manager, Regulatory Affairs & Market Development Bidgely Inc.

Manager, Regulatory Affairs iRhythm Holdings Inc

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

Senior Manager Regulatory Affairs contract Alumis Inc

Policy & Regulatory Affairs Manager Zoox

Manager, Regulatory Affairs iRhythm

Regulatory Affairs Manager F. Hoffmann-La Roche Ltd

Senior Manager, Regulatory Operations Nurix

Strategy and Operations Lead, Regulatory Affairs Google LLC

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

Sr. Manager, Regulatory Affairs Vaxcyte Inc

Sr. Manager, Regulatory Affairs Vaxcyte

Director of Regulatory Affairs and Policy SupplyBank.org

Senior Program Director, Commercial Regulatory Affairs Nesco Resource, LLC

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

Senior Manager, Regulatory CMC Vera Therapeutics Inc

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

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

Director, Regulatory Affairs Nurix Therapeutics Inc

Manager, Regulatory and Market Affairs Pattern Energy Group LP

Senior Program Director, Commercial Regulatory Affairs Integrated Resources, Inc

Senior Program Director, Commercial Regulatory Affairs Compass Consulting

Manager, Regulatory and Market Affairs Pattern Energy Group Inc

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

Director Regulatory Affairs - Cardiac Intuitive Surgical Inc

Senior Program Director, Commercial Regulatory Affairs SGA Inc.

Senior Program Director, Commercial Regulatory Affairs TalentBurst, Inc.

Manager, Regulatory Response Google LLC

Regulatory Systems Manager Ardelyx Inc

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

Senior Program Director, Commercial Regulatory Affairs Tailored Management

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