920 regulatory manager jobs at 465 companies in Compton, CA
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Regulatory Program Manager
El Segundo, California, United States
$161k-$236k/yrOnsiteFull Time
Radiant: Designs and manufactures portable, mass-produced nuclear microreactors.
5+ YOEBachelor's in engineering,5+ years in regulated industry (preferably nuclear/NRC or DOE),regulatory submission and licensing experience,strong written/verbal communication,ability to mentor junior staff,and willingness to work extended hours/weekends.
ALL4: Provides strategic environmental health and safety consulting services.
5+ YOEEngineering or environmental science degree; 5-30 years in environmental consulting; strong regulatory, permitting, and project management skills; California regulatory experience preferred.
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.
Huisong Pharmaceuticals: Manufacturer of natural ingredients for pharmaceutical and food industries.
5+ YOEBachelor's in a scientific field, 5+ years regulatory affairs experience in dietary supplements/botanicals/TCM, PCQI required, HACCP preferred, audit and FDA regulatory experience.
Los Angeles or Singapore or New York City or London or Dublin or Paris or Berlin or Dubai or Jakarta or Seoul or Tokyo
OnsiteFull Time
TikTok: Global short-form video hosting and social media platform.
5+ YOEProven program management delivering large cross-functional regulatory programs; knowledge of global digital platform regulations (e.g., DSA), risk assessment, stakeholder management, and executive communication.
BSH Home Appliances: Develops and manufactures major and small household appliances.
7+ YOE5+ MgmtBachelor's degree, project management certificate, 7+ years program/product management experience, 5+ years project leadership, experience with compliance, stakeholder management, and relevant IT tools.
Miro, Jira, SDD, Polarion, SAP, Pro Codex, Homologation DataBase, Team Center
Ritual: Sells science-backed vitamins with traceable ingredient supply chains.
5+ YOE1+ Mgmt5+ years regulatory affairs experience in supplements/consumer health, 1+ years people leadership, deep knowledge of FDA/FTC requirements, bachelor's in life science/pharmacy/food science, ability to manage regulatory submissions and label review.
John Paul Mitchell Systems: Sells professional-grade hair care products and styling equipment globally.
7+ YOE2+ Mgmt7+ years regulatory or packaging sustainability experience in CPG/beauty, 2+ years supervisory experience, bachelor’s degree, expertise in packaging sustainability, EPR, labeling and multi-market compliance.
PureTek: Manufactures pharmaceuticals, nutritional supplements, and personal care products.
1+ YOEBachelor’s in science or health field; 1-4 years in regulatory affairs or related PM/QA role; FDA/cGMP knowledge; strong organization; proficiency with MS Office and PM tools.
Microsoft Office, Monday.com, Asana, Veeva Vault, MasterControl
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.
Tarsus PharmaceuticalsNASDAQ: TARS: Developing therapeutics for eye care and infectious disease prevention.
8+ YOEBachelor’s degree in science or health-related field; 8+ years regulatory affairs experience, 5+ years on MLR/PRC committee; strong collaboration, detail-oriented, Veeva PromoMats Vault experience a plus; regulatory labeling/advertising oversight.
JenaValve Technology: Developing transcatheter heart valve systems for aortic disease treatment.
5+ YOEBachelor's in a scientific discipline, 5+ years medical device regulatory affairs experience, people management experience, expert knowledge of global regs for Class II/III devices, MDSAP and quality systems, and ability to interpret guidance and direct project teams.
RED Digital Cinema: Manufactures high-end digital cinematography cameras and professional video accessories.
10+ YOEBachelor's in a related field, 10+ years in chemical regulatory/compliance, strong knowledge of global regulations (REACH, TSCA, RoHS, Prop 65), experience with registrations, CMS and compliance documentation, strong communication and project skills.
Los Angeles or Atlanta or Cincinnati or Milwaukee or New York or Minneapolis or Chicago or Boston or Philadelphia or Denver or Charlotte
$139k-$164k/yrHybridFull Time
U.S. BankNYSE: USB: Provider of personal, business, and institutional financial services.
8+ YOELaw degree and license to practice in jurisdiction, 8+ years related experience, knowledge of the Investment Company Act of 1940, ability to manage teams and complex projects, strong communication and regulatory drafting skills.
Tarsus PharmaceuticalsNASDAQ: TARS: Develops and commercializes therapeutic treatments for prevalent ophthalmic diseases.
8+ YOE8+ years in regulatory affairs with MLR/PRC committee experience; Bachelor's in science or health-related field; strong regulatory knowledge; Veeva PromoMats experience a plus; team player with communication skills.
Veeva PromoMats, Regulatory Submissions, Regulatory Affairs Systems
UCLA Health: Provides comprehensive hospital services and academic medical research.
1+ YOEBachelor's degree or equivalent, 1+ years clinical research experience, knowledge of IRBs and regulatory requirements, strong interpersonal, analytical and organizational skills, ability to manage competing deadlines.
Adventist Health: Faith-based healthcare provider offering hospital and clinical services.
Bachelor's degree (or equivalent), HACP or CPHQ certification required within 2 years, experience in accreditation/regulatory compliance and leadership preferred, knowledge of accreditation/licensing standards and compliance processes.
Manager, United States Regulatory Strategy, General Medicine
Thousand Oaks or United States
$113k-$153k/yrRemoteFull Time
AmgenNASDAQ: AMGN: Develops and manufactures biotechnology medicines for serious diseases.
2+ YOEDegree (various levels) with related experience, regulatory submissions and FDA interaction experience preferred, knowledge of U.S. legislation/regulations for medicinal products, strong communication and risk assessment skills.
Flourish Research: Conducts multi-site clinical trials and patient research studies.
0+ YOEManage regulatory documents and submissions for clinical studies; high attention to detail, 0–3+ years clinical research experience, proficient with Microsoft Office, CTMS, eRegs/eDocs, strong written/verbal communication.
Microsoft Office (Outlook, Word, Excel), Office365, CTMS, eRegs/eDocs