San Francisco or Edina or Los Angeles or Philadelphia or Tampa or Denver or Seattle or New York City or Chicago
$105k-$193k/yrHybridFull Time
Marsh McLennanNYSE: MRSH: Provides global insurance brokerage, risk management, and professional consulting services.
3+ YOE3+ years insurance regulatory/filing experience (P&C) with California filings, ability to prepare regulator-ready materials, strong project management and communication, bachelor\u0002s or equivalent experience.
2+ YOEBachelor's degree required (Master's preferred),2+ years in higher education compliance/accreditation,knowledge of accreditation standards,project management and documentation skills,Microsoft Office proficiency.
Rainmaker: Provides cloud seeding services using drones and radar.
Experience preparing state/local environmental and permitting submissions, strong technical writing and communication, self-directed in fragmented regulatory environments, and willingness to travel domestically for meetings and hearings.
Scale Media: Builds and scales direct-to-consumer health and wellness brands.
2+ YOERequires 2–3 years of dietary supplement regulatory affairs experience, claims and label review experience, FDA/FTC knowledge, DSHEA and 21 CFR Part 111 familiarity, and a relevant bachelor's degree.
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/biological research experience; proficiency with Microsoft Office, CTMS, eRegs/eDocs; strong communication skills.
Microsoft Outlook, Microsoft Word, Microsoft Excel, CTMS, eRegs/eDocs, Office365
Broadata Communications: Manufactures hardware for high-speed multimedia transmission over fiber optics.
8+ YOE8-10 years in Regulatory Affairs/Quality within medical devices; hands-on Class I; FDA 21 CFR Part 820, ISO 13485; DHF/DMR, labeling, audits; cross-functional collaboration.
Sakura Finetek: Develops automated laboratory instruments and reagents for pathology labs.
3+ YOE3+ years medical device experience with ≥1 year in regulatory affairs; BA/S in science/engineering or equivalent; RA certification (RAC) a plus; knowledge of global regulations, QSR820, ISO 13485, IVDR; strong communication and analytical skills.
Caldera Medical: Developing surgical implants for women's pelvic health conditions.
1+ YOE1–3 years regulatory operations or related experience, advanced Excel, portal and registry experience (EUDAMED,GUDID), strong data discipline, attention to detail, ability to follow SOPs, bachelor’s degree or equivalent experience, onsite in Westlake Village, CA.
Acrobat, OCR, EUDAMED, FDA GUDID, Swissmedic, eSTAR, RIM, Microsoft Excel
Marlborough or Irvine or Arden Hills or Maple Grove
$89k-$170k/yrHybridFull Time
Boston ScientificNYSE: BSX: Developing and manufacturing innovative medical devices for less-invasive treatments.
4+ YOEBachelor’s degree in a scientific or technical discipline, 4+ years of medical-industry regulatory affairs experience, and experience with 510(k), EU MDR, or international regulatory registrations.
City of Hope: Medical research and treatment center for cancer and diabetes.
2+ YOEPrepare and review regulatory submissions, support investigators and manufacturing/QC/QA teams, draft SOPs and protocols; 2+ years regulatory experience with Bachelors (or 0–2 with Masters).
EnvistaNYSE: NVST: Manufactures and sells a comprehensive range of dental products.
2+ YOEBachelor's degree, 2+ years regulatory affairs experience in medical devices (or Master's +1 year). Strong EU MDR knowledge (CER, SSCP, PSUR, PMS). Experience with international submissions and regulatory strategy.
Kaiser Permanente: Provides integrated medical care and health insurance plans.
3+ YOEBachelor's degree or 3+ years clinical research experience; working knowledge of FDA/IRB regulations; preparing regulatory submissions, maintaining study documentation, and supporting quality assurance; BLS and clinical research certifications preferred.
Glidewell: Designs and manufactures custom dental restorations and laboratory products.
5+ YOE5+ years regulatory affairs experience, experience with FDA 510(k)/PMA and international registrations, SOP and audit experience, strong analytical and communication skills.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Outlook
Irvine or Marlborough or Arden Hills or Maple Grove
$89k-$170k/yrHybridFull Time
Boston ScientificNYSE: BSX: Developer and manufacturer of innovative medical devices and therapies.
4+ YOEBachelor's degree in a scientific, technical, or related discipline and 4+ years of medical industry regulatory affairs experience, including 510(k), EU MDR, or international registrations.
Ventura Foods: Manufactures custom food solutions for foodservice and retail businesses.
3+ YOE3+ years' regulatory compliance experience in food/beverage/pharmaceutical, knowledge of global food laws, label and ingredient compliance, strong communication and project leadership skills.
Microsoft Office, PIM, Decernis gComply, Decernis gComply Plus, Trustwell/Genesis
Western Funding: Provides automobile financing and loan servicing to car dealerships.
Knowledge of multi-state auto finance regulatory requirements and consumer financial protection laws; strong verbal and written communication; detail oriented; Bachelor's degree in business required; auto finance experience preferred.
Daybreak, Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Vision, web-based application
3+ YOE3+ years regulatory experience in cosmetics/pharma/consumer goods, Bachelor's in life sciences/pharmacy/chemistry, Mandarin proficiency, Microsoft Office skills, ability to work onsite 60%+ and manage international product registrations.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
StrykerNYSE: SYK: Manufactures medical devices and equipment for healthcare providers.
4+ YOEBachelor's in engineering, life sciences, regulatory science or related; minimum 4 years regulatory affairs experience in medical device/biotech/pharma; experience with international submissions and interpreting global regulations.