1,519 regulatory manager jobs at 600 companies in Ewing, NJ
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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/yr RemoteFull Time
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.
Slack, Apple macOS, GSuite
3w
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Manager Regulatory Affairs
Berkeley Heights, New Jersey, United States
$145k-$165k/yr OnsiteFull Time
8+ YOE8+ years regulatory affairs experience with ANDA submissions for sterile injectables, bachelor’s in pharmacy/chemistry/biology required, B.S. required; advanced degree/MBA preferred, strong written/oral communication and regulatory CMC expertise.
eCTD
2d
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Manager, Regulatory CMC
Somerset or Bridgewater
$127k-$167k/yr HybridFull Time
5+ YOEBachelor's degree in a relevant life science or engineering field, 5+ years of biotechnology or pharmaceutical experience, and 1–2 years of Regulatory CMC experience. Strong technical writing, scientific analysis, project management, and collaboration skills required.
CAR-T, TCR-T, NK, IND, CTA, BLA, MAA, FDA, EMA, ICH, E-Verify, Form I-9
3w
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Senior Manager EU Regulatory
Allentown, Pennsylvania, United States
HybridFull Time
10+ YOE10+ years energy industry experience with regulatory, rate, procurement and financial expertise; Bachelor's degree required; MBA/master's preferred; strong decision-making and leadership skills.
5d
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Regulatory Affairs Manager
Exton, Pennsylvania, United States
HybridFull Time
8+ YOEBachelor's degree with 8+ years or master's/PhD with 3+ years in regulated healthcare technologies; expertise in medical device software, cybersecurity, regulatory strategy, submissions, and digital health.
IEC 62304, IEC 82304, ISO 14971, Title 21 CFR, EU MDR 2017/745
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Manager, Regulatory Affairs
California or Los Angeles or Los Angeles County or San Francisco or Philadelphia or United States
$113k-$154k/yr OnsiteFull Time
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.
2mo
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Manager, Regulatory Affairs
Edison or United States or Canada or Australia
$99k-$125k/yr RemoteFull Time
7+ YOE5+ MgmtBachelor's in science or equivalent, 7+ years experience, 5+ years managerial experience, 5+ years in human tissue or medical device manufacturing, strong knowledge of FDA/QSR/cGMP/ISO, experience with FDA inspections and regulatory submissions; up to 20% travel.
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Product and Regulatory Implementation Manager
Philadelphia, Pennsylvania, United States
OnsiteFull Time
5+ YOEBachelor’s degree and 5 years of product development, regulatory implementation, or project management experience, preferably in healthcare; expertise in complex projects, cross-functional work, systems integration, migration, and testing.
Microsoft Project, Jira, SIT, UAT
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Manager, Regulatory Affairs - Cosmetics (Global)
Princeton, New Jersey, United States
$111k-$158k/yr HybridFull Time
8+ YOEBachelor's degree, 8+ years regulatory affairs experience in cosmetics, experience with NPD and lifecycle change control, regulatory master files and dossiers, project management, and strong communication skills.
Regulatory Information Management Systems (RIMS)
2w
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Manager, Technical Regulatory Compliance
Raynham or West Chester or Palm Beach Gardens
HybridFull Time
6+ YOEBachelor's degree required, typically 6+ years regulatory compliance/quality/engineering experience in a regulated industry; audit and inspection experience, regulatory interpretation, risk management, and strong communication skills.
1mo
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Manager, Regulatory Affairs - Cosmetics (Global)
Princeton, New Jersey, United States
$111k-$158k/yr RemoteFull Time
8+ YOEBachelor's degree and 8+ years of cosmetic regulatory affairs experience required, including global regulations, NPD launch readiness, lifecycle change control, regulatory dossiers, project management, and cross-functional leadership.
Regulatory Information Management Systems (RIMS)
2mo
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Regulatory Affairs Project Manager
Piscataway, New Jersey, United States
$124k-$174k/yr HybridFull Time
7+ YOEBachelor's in life sciences/quality/regulatory required; 7+ years in regulatory/compliance (2+ years project management); strong knowledge of ISO 13485, ISO 14971, FDA 21 CFR 820; eQMS/DMS and Smartsheet proficiency.
Smartsheet, GreenlightGuru, electronic Quality Management Systems (eQMS), document management systems (DMS)
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Regulatory Affairs Compliance Manager
The Woodlands or Parsippany
$107k-$190k/yr OnsiteFull Time
5+ YOECollege degree and 5+ years managing ISCC compliance for renewable fuel production. Requires regulatory interpretation, mass balance and GHG calculations, audit management, analytical skills, and Microsoft Office proficiency.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Outlook, RightAngle
2mo
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Regulatory Specialist
Fairfield, New Jersey, United States
$90k-$100k/yr OnsiteFull Time
Experience in regulatory affairs for cosmetics or nutrition, managing customer documentation portals, FDA compliance, KPI tracking, and cross-functional collaboration. Familiarity with regulatory databases and stakeholder communication; bachelor's in chemistry/biology preferred.
Salesforce, AODocs, PCPC, CIR, TSCA, EPA, Health Canada, EWG, VEEVA Vault
2mo
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Senior Manager, Regulatory Operations
Princeton, New Jersey, United States
$150k-$224k/yr OnsiteFull Time
7+ YOEMinimum 7 years regulatory operations experience with eCTD submissions, knowledge of FDA/EMA/Swiss Medic guidance, Documentum and publishing tools, Microsoft Office/SharePoint proficiency, staff supervision and vendor coordination.
Documentum, DocuBridge, InSight Publisher, GlobalSubmit Validate, GlobalSubmit Review, ISIToolbox, eCTD, Microsoft Word, Microsoft Excel, Microsoft Access, Microsoft PowerPoint, Microsoft SharePoint
2w
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US Regulatory Affairs Senior Manager – Allergy
Morristown, New Jersey, United States
$184k-$265k/yr HybridFull Time
5+ YOEBachelor's degree and 5–8 years of regulatory affairs experience required, including 4+ years supporting OTC NDA drugs and knowledge of U.S. regulatory submissions, labeling, and product lifecycle management.
NDA, ANDA, U.S. FDA
2mo
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Senior Manager, Regulatory Affairs - OTC
Warren, New Jersey, United States
$153k-$210k/yr HybridFull Time
7+ YOEBachelor's in pharmaceutical/life sciences required, 7+ years regulatory affairs experience (FDA/OTC/CMC), proven leadership, FDA interaction experience, strong communication and project management skills.
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1940 Act Regulatory Administration Manager
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/yr HybridFull Time
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.
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Associate Manager, Regulatory Affairs
Florham Park, New Jersey, United States
OnsiteFull Time
6+ YOEBachelor's degree preferred in life science, six years of relevant experience, English proficiency, FDA regulatory knowledge, original ANDA experience preferred, and proficiency with office, regulatory, database, and eCTD tools.
Microsoft Office Suite, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Microsoft Teams, Microsoft SharePoint, Adobe Acrobat, Electronic Common Technical Documents (eCTD), eCTD Compilation software, database systems
2d
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Regulatory Affairs Project Manager
Branchburg or Indianapolis or Tucson or Asia or South America or Africa
$93k-$173k/yr HybridFull Time
5+ YOEBachelor's or master's degree in life science, data science, or related field; 5 years' experience in regulatory, clinical, quality, development, or program management in IVD, medical device, or pharmaceutical industries.
Robotic Process Automation (RPA), AI, MedTech Regulatory Information Management System, CE IVD, MD, IDE, 510(k), PMA
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