104 regulatory specialist jobs at 65 companies in Fall River, MA
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Senior Regulatory Specialist
Marlborough, Massachusetts, United States
$89k-$111k/yr HybridFull Time
4+ YOEBachelor's degree in a relevant field, 4+ years regulatory medical device experience, authorized to work in the US, knowledge of ISO 13485/9001, experience with 510(k) submissions, and proficiency with Microsoft Office.
Microsoft Office, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
3d
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Clinical Regulatory Specialist
New York City or Cambridge or Southlake or United States or Europe or Asia or Australia
HybridFull Time
2+ YOERequires 2+ years in clinical research, regulatory affairs, or clinical operations; experience with Phase 2–4 trials, GCP, FDA requirements, IRB processes, SOPs, regulatory documents, and clinical research technology.
Clinical Trial Management System (CTMS), electronic regulatory platform, eSource
1w
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Federal Regulatory Specialist
Boston, Massachusetts, United States
$80k-$120k/yr OnsiteFull Time, Temporary
Requires federal rail regulatory compliance, FTA funding regulations, GAAP, financial and business planning, audits, reporting, regulated HR experience, and a bachelor's degree in a related field.
Generally Accepted Accounting Principles (GAAP)
3mo
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Regulatory & Clinical Specialist
Chicago or Atlanta or Austin or Denver or Houston or Phoenix or Boston or Minneapolis or Charlotte or Dallas or United States
$85k-$95k/yr RemoteFull Time
5+ YOESupport EU MDR and US regulatory submissions; develop CEP/CER; conduct literature reviews; liaison with regulatory authorities and internal teams.
Medical writing, Regulatory submissions, Literature databases
2mo
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Senior Regulatory Affairs Specialist
Marlborough or Irvine or Arden Hills or Maple Grove
$89k-$170k/yr HybridFull Time
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.
Microsoft Office
4w
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Senior Regulatory Affairs Specialist
Marlborough or Maple Grove
$89k-$170k/yr HybridFull Time
4+ YOEBachelor's in a scientific/technical discipline, 4+ years regulatory affairs experience in medical devices, experience with implantable/active devices, regulatory submissions and design controls, knowledge of FDA/EU regulations.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
4w
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Senior Regulatory Affairs Specialist
Marlborough or Maple Grove
$89k-$170k/yr HybridFull Time
4+ YOEBachelor's in a scientific/technical discipline, 4+ years regulatory affairs experience in medical devices, experience with implantable/active devices, regulatory submissions and FDA/EU requirements, strong writing and cross-functional collaboration skills.
Microsoft Word, Microsoft Excel, PowerPoint
3w
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Regulatory Escalation Specialist Intermediate
Johnston, Rhode Island, United States
HybridFull Time
3+ YOEBachelor's in business or related field, minimum 3 years relevant experience, ability to lead cross-functional teams, strong analytical and organizational skills; knowledge of regulatory frameworks preferred.
3w
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Regulatory Escalation Specialist Intermediate
Johnston, Rhode Island, United States
OnsiteFull Time
3+ YOEBachelor's degree in business or related field, minimum 3 years' relevant experience, strong regulatory knowledge, analytical and communication skills, ability to manage escalations and cross‑functional projects.
3d
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Sr Regulatory Affairs Specialist
Boston, Massachusetts, United States
$101k-$127k/yr HybridFull Time
3+ YOEBachelor’s degree with 3+ years’ experience or master’s degree with 1+ year; regulatory submissions experience, FDA IVD knowledge, scientific data interpretation, strong communication, collaboration, negotiation, and problem-solving skills.
FDA, Center for Devices and Radiological Health (CDRH), HIPAA
2mo
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Regulatory Reporting & Compliance Specialist
Keene or Madison or Boston
$62k-$103k/yr HybridFull Time
5+ YOEExperience in regulatory/stat reporting, SQL/BigQuery and Microsoft Excel expertise, knowledge of state insurance laws and rate/form filings, ability to reconcile datasets, and 5+ years in regulatory compliance or insurance preferred.
SQL, BigQuery, GCP, Microsoft Excel, Jira, Microsoft PowerPoint
2w
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Regulatory Affairs Specialist II, Expansion
Boston, Massachusetts, United States
$120k-$160k/yr OnsiteFull Time
4+ YOE4+ years regulatory affairs experience for medical device or digital health, EU MDR and IEC 62304 knowledge, experience with international submissions, strong communication and project management.
1mo
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Regulatory Reporting & Compliance Specialist
Keene or Boston or Madison
$62k-$103k/yr HybridFull Time
5+ YOERequires regulatory compliance and insurance experience, knowledge of state insurance laws, SQL/BigQuery, advanced Excel, data reconciliation, process documentation, analytical skills, and cross-functional collaboration.
SQL, Google BigQuery, Microsoft Excel, Jira, Microsoft PowerPoint
3w
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Regulatory Specialist for Center for Anesthesia Research Excellence
Boston, Massachusetts, United States
$60k-$88k/yr OnsiteFull Time
1+ YOEBachelor's degree required (Master's preferred),1-3 years regulatory or clinical research experience, knowledge of FDA/NCI/OHRP guidelines, ability to maintain confidentiality, and proficiency with web-based systems and Microsoft Office.
Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Access
3d
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Regulatory Remediation Specialist – Risk & Governance Vice President
Boston or Quincy
$120k-$203k/yr OnsiteFull Time
Regulatory remediation experience in technology, cybersecurity, risk, or governance; senior individual-contributor experience in regulated environments; strong writing, technical aptitude, organization, prioritization, and stakeholder management skills.
2mo
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Usability and Regulatory Affairs Specialist
Lincoln, Rhode Island, United States
$90k-$110k/yr OnsiteFull Time
3+ YOE3+ years in human factors/usability or regulatory affairs in medical devices; Bachelor's in biomedical engineering or related; strong technical and analytical skills; familiarity with FDA and EU MDR preferred; ability to travel ~5 trips/year.
1mo
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Prin Regulatory Affairs Spec
North Haven or Mansfield or Mounds View or Boston or Lafayette
$120k-$180k/yr OnsiteFull Time
7+ YOEBachelor's degree, minimum 7 years regulatory experience (or advanced degree with 5+ years), experience with 510(k)/FDA interactions preferred, knowledge of medical device regulatory lifecycle, strong communication and cross-functional collaboration skills.
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Prin Regulatory Affairs Spec
North Haven or Mansfield or Mounds View or Boston or Lafayette
$120k-$180k/yr OnsiteFull Time
7+ YOEBachelor's degree and 7+ years regulatory experience (or advanced degree with 5+ years). Experience with 510(k), FDA interactions, international registrations, labeling and promotional material review.
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Lead Environmental Regulatory Specialist/Project Manager
Marion or Massachusetts or Rhode Island or United States
$110k-$130k/yr HybridFull Time
10+ YOEBachelor's in a related field, minimum 10 years environmental engineering experience, proven permitting experience (MA & RI), EPA NPDES knowledge, project management, regulatory and coastal/waterfront construction expertise.
1w
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Senior Regulatory and Scientific Affairs Specialist (Remote)
Bridgewater or Dallas or Boston or Chicago or San Diego or New Jersey
$85k-$110k/yr RemoteFull Time
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.
SAP, ContentHub, Veeva
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