395 regulatory manager jobs at 201 companies in Poway, CA
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Senior Regulatory Compliance Manager
San Francisco or Salt Lake City or Phoenix or Los Angeles or Chicago or Boston or Austin or New York City or Miami or Tampa or Atlanta or Columbus or Boise or San Diego or Minneapolis or Houston or Raleigh or Nashville or Kansas City or Charlotte or Portland or Philadelphia or Dallas or Washington or Seattle
$173k-$223k/yrRemoteFull Time
CircleNYSE: CRCL: Digital currency issuer and blockchain financial infrastructure provider.
10+ YOERequires 10+ years in financial institution compliance or regulatory work, compliance program implementation, regulatory change management, regulatory analysis, cross-functional leadership, and familiarity with Slack, Apple MacOS, and GSuite.
Neurocrine BiosciencesNASDAQ: NBIX: Develops pharmaceuticals for neurological, endocrine, and psychiatric disorders.
2+ YOE2+ MgmtDegree in life/health sciences (BS/MS/PharmD/PhD) with 2–6+ years industry experience (regulatory experience required), knowledge of FDA/ICH guidance, project management, leadership, and strong communication skills.
Travere TherapeuticsNASDAQ: TVTX: Developing and selling therapies for rare kidney diseases.
6+ YOE6+ years regulatory affairs experience in pharma/biotech; bachelor\u0002s in life sciences required (advanced degree preferred); experience with IND/CTA and global submissions; knowledge of FDA/EMA/ICH; ability to travel up to 10%; able to perform onsite work in San Diego.
ErascaNASDAQ: ERAS: Developing precision oncology medicines to treat cancer patients.
5+ YOEUndergraduate degree required (advanced preferred),5+ years regulatory affairs experience in pharma/biotech, experience with IND/CTA and global submissions, strong organization, communication, and regulatory knowledge.
Axos FinancialNYSE: AX: Provides digital-first banking and diverse financial services to customers.
10+ YOE5+ Mgmt10+ years in banking/financial services or compliance,5+ years leading RegTech or compliance technology,experience with AI, automation, analytics, and regulatory programs.
Microsoft Copilot, Power BI, Tableau, SQL, Python, Power Automate, n8n, Salesforce, Archer, ServiceNow, GRC platforms, AI/LLM technologies
Synchron: Developing implantable brain-computer interfaces to restore functional independence.
12+ YOEBachelor's in engineering/life sciences required (advanced preferred); 12+ years regulatory affairs in medical devices with Class III implantable device experience; track record of IDE/PMA submissions; software/firmware and AI/ML regulatory expertise; knowledge of 21 CFR parts.
Principal Regulatory Affairs Specialist – Vascular (on-site)
Santa Clara or Temecula
$100k-$200k/yrOnsiteFull Time
AbbottNYSE: ABT: Provides medical devices, diagnostics, and science-based nutritional products.
6+ YOEBachelor's in a scientific discipline, regulatory submissions experience for medical devices, knowledge of 21 CFR 820 and ISO 13485, experience with FDA and EU MDR submissions, ability to manage programs and cross-functional teams; 6+ years preferred.
Director / Senior Director of Regulatory Operations
San Diego, California, United States
$205k-$268k/yrHybridFull Time
Artiva BiotherapeuticsNASDAQ: ARTV: Develops allogeneic natural killer cell-based therapies for various diseases.
15+ YOE5+ Mgmt15+ years regulatory affairs/operations experience with 5+ years leadership; deep eCTD and Veeva Vault RIM expertise; proven end-to-end global submission delivery; SOPs and RIM ownership.
8+ YOEAdvanced degree preferred (MD/PhD/PharmD), 8+ years pharma experience with 6+ years in regulatory affairs, global regulatory expertise, drug development knowledge, strong communication and leadership skills, ability to interface with health authorities.
AECOMNYSE: ACM: Provides infrastructure consulting and engineering services for global projects.
6+ YOEBA/BS +6 years (or equivalent) experience; experience with California school facility funding, grant application preparation, financial/project management systems, familiarity with OPSC and CDE online systems, strong research, analytical, and communication skills, Excel.
Principal Regulatory Affairs Specialist – Vascular (on-site)
Santa Clara or Temecula
$100k-$200k/yrOnsiteFull Time
AbbottNYSE: ABT: Manufactures medical devices, diagnostics, and nutritional health products.
Bachelor's in science, experience preparing regulatory submissions for medical devices, knowledge of FDA/EU/ISO requirements, and familiarity with QMS; 6+ years preferred.
8+ YOEBS/MS/PhD in science, engineering, or management and 8+ years pharmaceutical/biopharmaceutical experience with regulatory filings and material specifications; expert knowledge of ICH, ISO, GMP, and operational excellence tools.
Colorado Springs or Nashville or Bothell or Gainesville or San Diego or Plymouth or Cambridge
$162k-$258k/yrHybridFull Time
PhilipsEuronext Amsterdam: PHIA: Manufactures medical imaging systems and personal care appliances.
15+ YOE15+ years in FDA-regulated medical device environments, leadership in quality/regulatory and M&A, Bachelor's required (Master's/MBA preferred), knowledge of FDA/ISO/EU MDR, QMS and KPI-driven governance.
Arrowhead PharmaceuticalsNASDAQ: ARWR: Develops RNAi medicines to treat genetic and intractable diseases.
8+ YOEBachelor's in life/computer/related science; 8+ years in biotech/pharma leading product labeling across multiple regions; knowledge of FDA guidance and advertising/promotion regs; strong document review, negotiation, and formatting skills.
Senior Regulatory and Scientific Affairs Specialist (Remote)
Bridgewater or Dallas or Boston or Chicago or San Diego or New Jersey
$85k-$110k/yrRemoteFull Time
NestléSIX Swiss Exchange: NESN: Produces and sells a wide range of food and beverages.
4+ YOEBachelor's degree in food science, nutrition, chemistry, or related science; 4+ years in food or supplement regulatory work; project management, compliance, and problem-solving skills; national travel availability.
New York City or Santa Monica or Los Angeles or Palo Alto or Chicago or Washington or Boston or Colorado or Seattle or San Francisco or San Diego or Reston
$170k-$240k/yrOnsiteFull Time
Cooley: Provides legal counsel to technology and life sciences companies.
7+ YOE2+ Mgmt7+ years relevant experience with 2+ years management experience; proficiency with Microsoft Office, PowerPoint, Excel and iManage; ability to travel and work extended/weekend hours; strong leadership and marketing strategy skills.
Microsoft Office, Microsoft PowerPoint, Microsoft Excel, iManage, CRM