283 regulatory manager jobs at 156 companies in Eliot, ME
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Regional Regulatory Manager
Billerica, Massachusetts, United States
$104k-$156k/yr HybridFull Time
1+ YOEAdvanced degree such as PhD, PharmD, or MD; at least 1 year of US drug development regulatory strategy experience; FDA interaction experience and matrix leadership skills.
FDA
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Regional Regulatory Manager
Billerica, Massachusetts, United States
$104k-$156k/yr HybridFull Time
1+ YOEAdvanced degree such as PhD, PharmD, or MD; at least 1 year of US drug development regulatory strategy experience; FDA interaction experience; and demonstrated matrix leadership skills.
FDA
2mo
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Senior Manager, Regulatory Accounting
Westlake or Merrimack
OnsiteFull Time
Expertise in mutual fund operations, accounting, or regulatory reporting; knowledge of alternative investments; leadership, stakeholder influence, analytical skills, and InvestOne and Microsoft Office experience.
InvestOne, Microsoft Office
3d
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Manager, Regulatory Operations (Publishing)
Woburn, Massachusetts, United States
$138k-$169k/yr HybridFull Time
8+ YOEBachelor's degree required; 8+ years of regulatory operations and publishing experience in biotechnology, pharmaceuticals, or related industries; expert Veeva Vault RIM expertise and global submission leadership required.
Veeva Vault RIM Submissions, Veeva Vault RIM Publishing, SEND, Veeva PromoMats, DXC, eCTD Xpress, ISI Toolbox, Lorenz, StartingPoint, eCTD, CTIS
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Associate Manager CMC Regulatory Compliance
Billerica, Massachusetts, United States
$78k-$117k/yr HybridFull Time
1+ YOEBachelor's in life science, 1+ years pharmaceutical or regulatory/CMC experience; experience preparing CMC dossiers, regulatory strategy, and health authority interactions; strong writing and communication skills.
2w
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Analyst III, Regulatory Accounting
Gainesville or Downey or Joplin or Londonderry or Merrick or Tahoe Vista or Litchfield Park
$80k-$115k/yr HybridFull Time
5+ YOEBachelor's degree and 5–8 years of accounting or regulatory experience. Requires US GAAP, utility accounting, regulatory reporting, advanced Excel, analytical, communication, and stakeholder management skills.
Microsoft Excel, SAP, Hyperion/HFM, Workiva, Power BI, PowerPlan, BlackLine, FERC Form 1, FERC Form 3-Q, US GAAP, FERC USOA, NARUC
4d
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Coordinator Regulatory Compliance Environmental
Woburn, Massachusetts, United States
$26-$31/hr HybridFull Time
Associate or bachelor's degree in environmental science or similar preferred; project, database, and file management experience preferred; regulatory knowledge, communication, organization, and cross-functional collaboration skills required.
Oasis, Oracle, Remedy
6d
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Vice President, Regulatory Affairs, SS
Princeton or Plainsboro or Mansfield or Cincinnati or Añasco or Columbia or United States or Braintree or Billerica
$225k-$316k/yr OnsiteFull Time
15+ YOE5+ MgmtBachelor's degree in a technical field and 15+ years in an FDA-regulated industry, or equivalent advanced-degree experience; 5+ years managing people or leading teams preferred. MedTech regulatory strategy expertise required.
510(k) Premarket Notifications, IDE, PMA, Design Dossiers, Technical Files, FDA, ISO, EU MDR
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Regulatory Affairs Project Manager
Manchester, New Hampshire, United States
OnsiteFull Time
5+ YOEBS in technical field,5+ years regulatory experience in medical device/drug/biologic,experience with FDA submissions (510(k),PMA,IDE),eSTAR,QMS/ISO13485/MDSAP knowledge,strong written/verbal skills.
eSTAR
2mo
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Risk Manager II, Accreditation, Regulatory Ops, Pharmacy
Manchester or Austin or Phoenix or Plainfield
$74k-$130k/yr OnsiteFull Time
Experience in project management, drafting policies/SOPs, knowledge of NABP/URAC/ACHC/LegitScript, auditing or compliance background, strong communication and documentation skills.
Microsoft Outlook, Microsoft Word, Microsoft Excel
2mo
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Permitting & Regulatory Compliance Specialist II
Charlotte or King of Prussia or Scottsdale or Frisco or Bellevue or Wyoming or Iowa or Mississippi or Idaho or Roseville or Richland or Puyallup or Klamath Falls or Chehalis or Kansas or Long Beach or Minnesota or Kent or Utah or Kentucky or Nevada or Massachusetts or Georgia or Arkansas or Ohio or Michigan or Missouri or Connecticut or Illinois or Pennsylvania or Delaware or Philadelphia or Burlington or North Carolina or Wisconsin or Louisiana or Oregon or Maryland or Texas or Bentonville or Oklahoma or Farmers Branch or Minneapolis or Ontario or Somerville or West Chester or Tennessee or Colorado or Arizona or Tampa or Virginia or Hillsboro or Maine or New Jersey or South Carolina or Indiana or Alabama or New Hampshire or Washington or New Mexico or Florida or California or Naperville or Duluth or Saint Louis
$35-$45/hr HybridFull Time
4+ YOEHigh school diploma, 4+ years permitting/compliance experience (4–6+ preferred), experience in A/E/C or related fields, permitting (UST/air quality) experience a plus, Microsoft Office proficiency, strong project/time management and client-facing skills.
Microsoft Office, Microsoft Excel, Microsoft Word, Microsoft Outlook
1w
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Vice President of Quality & Regulatory
Wilmington, Massachusetts, United States
OnsiteFull Time
12+ YOE5+ MgmtBachelor's or master's degree in engineering, life sciences, or a related technical field; 12+ years of regulated medical-device quality leadership, including 5+ years leading a substantial quality organization or function.
Statistical Process Control (SPC)
2mo
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Project Manager
Wilmington, Massachusetts, United States
$100k-$125k/yr OnsiteFull Time
5+ Mgmt5+ years supervision/management experience, active Massachusetts drinking water treatment and distribution licenses, HS diploma or equivalent, valid driver’s license, Windows PC familiarity, regulatory reporting, sampling, troubleshooting, and maintenance skills.
Microsoft Windows
1mo
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Principal Product Manager
Burlington, Massachusetts, United States
OnsiteFull Time
10+ YOE10+ years B2B SaaS product management with 3+ years owning a product line, enterprise/regulatory experience (financial services), AI/ML product experience, strong discovery and executive communication, US-based with ~15–20% travel.
Salesforce, Microsoft 365, Exchange, Google Workspace, Zoom, Microsoft Teams
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Credit & Debit Card Product Manager
Portland or Middletown
OnsiteFull Time
5+ YOE5+ years in card product management or financial product strategy; bachelor\u0002s required (master\u0002s preferred); expertise in card KPIs, P&L, forecasting, vendor negotiation, and regulatory compliance.
Microsoft Excel, Tableau, Microsoft Power BI
1w
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Environmental Project Manager
Concord or New Hampshire
$88k-$144k/yr OnsiteFull Time
7+ YOE3+ MgmtBachelor’s degree in civil or environmental engineering, geology, or environmental sciences; 7–10 years of environmental experience; 3+ years managing environmental consulting projects; regulatory and team leadership expertise.
1mo
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Program Manager, New Product Development
Andover, Massachusetts, United States
$147k-$184k/yr OnsiteFull Time
8+ YOEBachelor's in engineering or life sciences required,8+ years program/project management in medical device or regulated industry,PMP preferred,knowledge of FDA/ISO regulatory requirements,experience with design control and lifecycle management.
Microsoft Project, Smartsheet, JIRA
2mo
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Project Manager
Burlington or Bedford or Boston or Horsham or Wilmington
$105k-$125k/yr HybridFull Time
8+ YOEBachelor's degree in engineering or related field, 8+ years air permitting and regulatory compliance experience, strong communication, Excel proficiency, valid driver’s license; PE preferred.
Microsoft Excel
2mo
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Sr. Global Product Manager
North Billerica, Massachusetts, United States
$145k-$160k/yr OnsiteFull Time
8+ YOEBachelor's degree required (MBA preferred), 8+ years product management in medical device/capital equipment, intraoperative imaging experience preferred, experience with global launches, regulatory, AI usage, cross-functional collaboration, and executive communication.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1mo
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Program Manager - Medical Device
Beverly or Baldwin Park
$120k-$140k/yr OnsiteFull Time
8+ YOEBachelor's in engineering/chemistry/biology, 8+ years in medical device, 6+ years program/project management in manufacturing, knowledge of ISO/GMP/regulatory (FDA/MDR/Health Canada/PMDA), DOE/Lean/Six Sigma experience.
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