1,260 regulatory manager jobs at 529 companies in Berkeley, CA
3w
Save
Mark Applied
Hide
3w
Manager, Regulatory Submission Management
Parsippany or Foster City
$124k-$160k/yrHybridFull Time
Gilead SciencesNASDAQ: GILD: Develops and sells medicines for life-threatening infectious diseases.
4+ YOE4+ years regulatory submission/operations experience (with MS) or 6+ years (with BS). Must manage global regulatory submissions, author submission documents, and collaborate cross-functionally; strong regulatory knowledge and project management skills required.
Microsoft Office, Smartsheet, Microsoft SharePoint
Gilead SciencesNASDAQ: GILD: Develops and sells medicines for life-threatening infectious diseases.
6+ YOEBachelor's with 6+ years or Master's with 4+ years regulatory submission or operations experience in biopharma; SME in global submission types, strong writing, project management, and familiarity with submission standards.
CloroxNew York Stock Exchange: CLX: Manufactures and markets consumer cleaning and wellness products.
8+ YOEBachelor's in a technical discipline and 8+ years in regulatory affairs/product stewardship with strong EPR and multi-jurisdictional regulatory experience; ability to interpret regulations, manage complex requirements, and communicate across functions.
Santa Monica or Foster City or El Segundo or Thousand Oaks
$133k-$172k/yrHybridFull Time
Kite PharmaNASDAQ: GILD: Developing engineered cell therapies to treat and cure cancer.
5+ YOEBS +7 years or MS +5 years regulatory affairs experience; in-depth knowledge of ICH and regional regulatory requirements; experience preparing regulatory submissions, labeling and packaging input; strong communication and organizational skills.
Nurix TherapeuticsNASDAQ: NRIX: Develops targeted protein degradation medicines for cancer and inflammation.
5+ YOEBachelor's in life sciences, 5+ years in regulatory affairs/operations, proficient with Veeva RIMS SCP and publishing tools (DocuBridge, GlobalSubmit, VeevaVault Submission), knowledge of 21 CFR/ICH/GCP/GMP/eCTD, MS Word/Excel/PowerPoint/Smartsheet.
Veeva RIMS SCP, Veeva RIMS, VeevaVault Submission, DocuBridge, GlobalSubmit, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Smartsheet
Manager, Global Regulatory Affairs Project Management
Redwood City, California, United States
$143k-$178k/yrHybridFull Time
Revolution MedicinesNASDAQ: RVMD: Developing precision oncology therapies for RAS-addicted cancers
5+ YOE3+ MgmtBachelor's in life sciences,5+ years pharma/biotech experience including 3+ years regulatory project management; knowledge of CTD,dossier management and global regulatory pathways; strong communication and project management skills.
Smartsheet, Microsoft Project, OnePager, Office Timeline, Veeva RIM
Indianapolis or Branchburg or Tucson or Santa Clara or Pleasanton or Carlsbad
$106k-$197k/yrOnsiteFull Time
RocheSIX Swiss Exchange: ROG: Develops and manufactures pharmaceutical medicines and diagnostic solutions.
3+ YOEBachelor’s/Master’s in Life Science or Data Science; 3-8 years in regulatory affairs across IVD/medical devices/pharma; knowledge of US/EU/China regulations; experience with complex regulatory product launches.
ORIC PharmaceuticalsNasdaq: ORIC: Develops oncology therapies addressing mechanisms of drug resistance.
6+ YOE6+ years regulatory affairs experience in pharma/biotech, bachelor’s in a scientific field (advanced degree preferred), experience preparing IND/DSUR/CTA and FDA meeting requests, strong writing and project management skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Veeva RIM
Jade BiosciencesNASDAQ: JBIO: Developing best-in-class therapies for autoimmune diseases.
5+ YOEBachelor's degree required; 5+ years pharma/biotech R&D experience including 3+ years in Regulatory Affairs; experience with IND and eCTD submissions, strong scientific interpretation, regulatory knowledge (FDA/ICH/EMA), and proficiency in MS Word, Excel, and Adobe Acrobat.
Microsoft Word, Microsoft Excel, Adobe Acrobat, eCTD
Braveheart Bio: Develops therapies for hypertrophic cardiomyopathy and cardiovascular disease.
5+ YOEBachelor's degree, 5+ years regulatory affairs experience in biotech/pharma with strong focus on EU and ex‑U.S. clinical trial submissions (CTIS/CTA); experience managing CROs, health authority interactions, and regulatory lifecycle activities.
Regulatory Compliance Program Manager, Regulatory Delivery & Transparency - Trust and Safety
San Jose, California, United States
$109k-$288k/yrOnsiteFull Time
TikTok: Global short-form video hosting and social media platform.
5+ YOEProven program management delivering complex cross-functional regulatory programs; deep knowledge of DSA/Online Safety Acts and global regulations; strong risk assessment, stakeholder management, and communication skills; flexible for global collaboration.
7+ YOE7+ MgmtJD or equivalent, 7+ years attorney-level experience, experience with legal/regulatory/litigation matters and managing teams, admitted to practice in the position state, B2 communication and strategic skills.
Vera TherapeuticsNASDAQ: VERA: Develops treatments for serious immunological and autoimmune diseases.
6+ YOEBA/BS in a scientific field with minimum 6 years of regulatory affairs experience; strong US regulatory knowledge; CMC development in biologics preferred; proficient in regulatory information management systems (Veeva Vault RIM a plus).
California or Los Angeles or Los Angeles County or San Francisco or Philadelphia or United States
$113k-$154k/yrOnsiteFull Time
Victoria's Secret & Co.NYSE: VSCO: Retailer of lingerie, apparel, and beauty products.
5+ YOEBachelor's degree in a relevant field and 5–7+ years regulatory affairs experience in cosmetics/personal care; strong knowledge of global cosmetic and packaging regulations; experience with global launches and submissions; cross-functional influence and mentoring skills.
Airwallex: Global financial platform for business payments and money management.
6+ YOEBachelor's degree and 6+ years regulatory compliance experience in financial services/FinTech/legal/consulting; familiarity with US/Americas financial regulations; data proficiency; strong communication; experience building compliance programs and licensing processes.
Ambrosia Energy: Building vertically integrated, high-speed solar and battery power plants
Bachelor's degree and regulatory/permitting experience; preferred 4+ years in permitting/regulatory affairs or project development for solar, wind, or battery storage; ERCOT/Texas experience a plus.
Xona Space Systems: Operates low Earth orbit satellites for high-precision navigation services.
7+ YOELead global regulatory and public policy initiatives; 7–15+ years in government affairs or regulatory policy; aerospace/space policy expertise; strong communication and diplomacy; willing to travel; hybrid onsite in Burlingame, CA or Washington, D.C.
Sutro BiopharmaNASDAQ: STRO: Develops clinical-stage antibody-drug conjugates for oncology and autoimmune diseases
5+ YOEBachelor's in Life/Health Sciences required; 5+ years pharma/biotech experience with ≥4 years in regulatory affairs. Experience with INDs/CTAs/BLAs/MAAs, regulatory agency interactions, strong communication, leadership, and analytical skills.
VaxcyteNASDAQ: PCVX: Developing vaccines to prevent and treat bacterial diseases.
9+ YOEDevelop and execute global regulatory CMC strategies, prepare and file CMC submissions, manage Health Authority interactions; BSc in a scientific discipline and 9+ years vaccine/biotech experience; experience with module 32S/32P and CMC DS sections (BLA/IND/IMPD).