527 regulatory manager jobs at 273 companies in Temple, PA
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Senior Manager EU Regulatory
Allentown, Pennsylvania, United States
HybridFull Time
10+ YOEBachelor's in finance/accounting/business/regulatory affairs/public affairs/law required; 10+ years energy industry regulatory experience; MBA or master’s preferred; regulatory accounting and leadership experience; knowledge of PUC/FERC and energy markets.
5d
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Manager, Regulatory Intelligence
Raynham or West Chester or Palm Beach Gardens or Warsaw or Raritan or Leeds or Ringaskiddy
$153k/yr HybridFull Time
6+ YOEBachelor’s degree required and 6–8 years’ Quality, Regulatory Affairs, or Standards Compliance experience in a regulated industry. Requires regulatory interpretation, QMS knowledge, cross-functional influence, and audit or inspection experience.
ISO 13485, ISO 14971, IEC, FDA QSR, EU MDR
5d
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Manager, Regulatory Intelligence
Raynham or West Chester or Palm Beach Gardens or Warsaw or Raritan or Leeds or Ringaskiddy
$153k/yr HybridFull Time
6+ YOEBachelor's degree and 6–8 years in quality, regulatory affairs, or standards compliance in a regulated industry. Requires regulatory interpretation, QMS knowledge, cross-functional influence, audit support, and strong analytical communication skills.
1mo
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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.
1w
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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
3w
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Manager, Regional Regulatory Lead - LCM
Waltham or King of Prussia
$129k-$153k/yr HybridFull Time
5+ YOEBachelor's degree in a relevant life science, 5+ years of biotech or pharmaceutical regulatory experience, 3+ years with developmental products, regional regulatory knowledge, and health authority interaction experience.
Veeva
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Senior Manager Regulatory Affairs CMC
Wilmington, Delaware, United States
OnsiteFull Time
In-depth CMC regulatory knowledge for small and large molecules, experience preparing eCTD submissions, degree in a scientific or regulatory field, and ability to liaise with global health authorities.
eCTD, electronic document management systems
2mo
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Senior Manager, Medical/Regulatory Writer
Gaithersburg or Radnor or United States
RemoteFull Time
3+ YOELead medical and regulatory writing for submissions from first‑in‑human through registration; strong writing track record, knowledge of global regulatory requirements, MS Word and Adobe Acrobat proficiency, experience with eDMS/RIMS and review systems; BS or advanced degree with relevant years of experience.
Microsoft Word, Adobe Acrobat, eDMS, RIMS, eCTD
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Biopharma Regulatory Strategist
King of Prussia, Pennsylvania, United States
$139k-$208k/yr OnsiteFull Time
15+ YOEAdvanced degree in life sciences or related field, 15+ years regulatory affairs experience in biopharma with deep CMC expertise, experience with FDA/EMA/PMDA, strong commercial acumen and executive communication.
3w
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Manager, Regional Regulatory Lead - LCM
Waltham or King of Prussia
$129k-$153k/yr HybridFull Time
5+ YOEBachelor's degree in a life science or related field; 5+ years regulatory or submission experience, 3+ years with developmental products, health authority knowledge, strategic thinking, and strong communication skills.
Veeva, FDA, EMA
2mo
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Associate Director Regulatory Affairs, Oncology
Upper Providence or Waltham or Rockville or Durham or Cambridge or San Francisco
$139k-$231k/yr HybridFull Time
Develop and execute regional regulatory strategies for oncology assets, lead regional submissions and interactions with regulatory authorities, ensure compliance across product lifecycle, and work cross-functionally within global matrix teams.
2mo
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Manager, Financial Statement and Regulatory Reporting
Malvern or Wayne
HybridFull Time
4+ YOE3+ Mgmt4+ years in accounting/finance roles, 3 years supervisory experience, strong U.S. GAAP and IFRS knowledge, regulatory reporting expertise (Form PF/SLT), advanced derivatives knowledge, bachelor's in Accounting/Finance/Economics; CPA/CFA/CA preferred.
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Director of Regulatory Affairs
Chesterbrook, Pennsylvania, United States
OnsiteFull Time
10+ YOE10–15 years regulatory affairs experience in biotech/pharma, bachelor's degree required (advanced degree preferred), experience with late-stage and biologics development, FDA interactions, and managing CROs/consultants.
2mo
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Director Promotional Regulatory Affairs
Wilmington, Delaware, United States
HybridFull Time
5+ YOEBachelor's in science required; 5+ years total pharma/biotech/FDA experience with 3+ years in promotional regulatory affairs or OPDP/APLB; strong knowledge of FDA promotional regulations, drug development, and labeling; experience engaging FDA.
AZAP
1w
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Mgr Site Regulatory Assurance
Middletown, Pennsylvania, United States
$162k-$180k/yr OnsiteFull Time
8+ YOERequires a technical bachelor's degree with 8 years' experience, or equivalent SRO, associate degree, or high school pathways with 8–12 years' experience; strong communication and access eligibility required.
Technical Specifications, Updated Final Safety Analysis Reports (UFSAR), Code of Federal Regulations
1w
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Assoc. Dir, Regulatory Affairs-CMC
Rahway or North Wales
$142k-$224k/yr HybridFull Time
5+ YOEBS or equivalent scientific, technical, or regulatory degree; 5+ years in pharmaceutical or biotech Regulatory CMC; hands-on digital, automation, and AI/LLM experience; change management, mentoring, collaboration, and project coordination skills.
Artificial Intelligence (AI), machine learning, generative AI, AI/LLM, Electronic Common Technical Document (eCTD), Veeva, ERA App
3w
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Head of Regulatory, AM & D
Cambridge or Malvern or Chicago
$171k-$291k/yr OnsiteFull Time
8+ YOE8+ years with bachelor's (or 6+ with master's) in regulatory affairs for medical devices, people leadership, 510(k) authoring experience, knowledge of ISO 13485/14971, RAC preferred, willingness to travel up to 15%.
1mo
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Mgr, Advocacy, Product Stewardship & Regulatory Affairs
Exton, Pennsylvania, United States
$125k-$145k/yr OnsiteFull Time
8+ YOEBachelor's degree required (advanced preferred),8+ years in regulatory/product stewardship/government affairs in chemicals,knowledge of TSCA/FIFRA/OSHA,stakeholder engagement,technical and policy writing.
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
3w
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Director, Regulatory Affairs, Advertising and Promotion
West Chester, Pennsylvania, United States
HybridFull Time
8+ YOEBachelor's in life sciences or pharmacy required; advanced degree preferred. 8+ years regulatory affairs experience with ≥6 years in advertising and promotion; deep FDA OPDP knowledge, Form 2253/eCTD/ESG experience, and strong communication and analytical judgment.
Veeva Vault PromoMats, Zinc MAPS, eCTD, ESG
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