638 regulatory manager jobs at 307 companies in Intercourse, PA
1d
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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
1d
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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.
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
1d
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Sr Manager, Regulatory Operations
Newark or Marlborough
$145k-$242k/yr OnsiteFull Time
10+ YOERequires a bachelor's degree and 10+ years of experience, or advanced-degree alternatives. Requires medical device regulatory expertise, FDA, ISO 13485, EU MDD/MDR knowledge, management experience, and strong communication skills.
FURLS, Eudamed, GUDID, ISO 13485, FDA Code of Federal Regulations (21CFR), EU MDD/MDR
2w
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Regulatory Compliance Manager
Hunt Valley, Maryland, United States
$103k-$186k/yr OnsiteFull Time
6+ YOE4+ MgmtBachelor's degree in a scientific or engineering discipline; 6+ years pharmaceutical or similar experience, including 4+ years in quality assurance or compliance management and 3+ years in sterile manufacturing and aseptic filling.
Electronic Quality Management System (eQMS), FDA Form 483, ISO 14644
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Regulatory Compliance Manager
Hunt Valley, Maryland, United States
$103k-$186k/yr OnsiteFull Time
6+ YOE4+ MgmtBachelor’s degree in a scientific discipline; 6+ years in pharmaceutical or similar industry; 4+ years in quality assurance or compliance management; 3+ years in sterile manufacturing and aseptic filling; audit and eQMS experience.
Electronic Quality Management System (eQMS), FDA Form 483, ISO 14644, ALCOA+
2w
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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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Regulatory Specialist
Laurel or Baltimore or Maryland or Colorado or Hawaii or Illinois or California or New Jersey
$80k-$117k/yr HybridFull Time
8+ YOE8+ years regulatory environmental experience, knowledge of Maryland and federal regulations, permitting application management, advanced technical writing and agency coordination, field survey leadership, and proficiency with Microsoft Office; CADD/GIS a plus.
Microsoft Word, Microsoft Excel, Microsoft Outlook, CADD, GIS, GPS
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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.
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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
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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.
3mo
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Sustaining & Compliance Projects Senior Manager, Regulatory Affairs
Sparks, Maryland, United States
$150k-$239k/yr OnsiteFull Time
7+ YOE5+ Mgmt7+ years in QA/Regulatory Affairs; 5+ years of management; project management; cross-functional leadership; regulatory submissions knowledge; clinical diagnostics knowledge preferred
Regulatory information management, Quality Management System (QMS) knowledge
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.
2mo
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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.
1mo
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Director Promotional Regulatory Affairs
Wilmington, Delaware, United States
HybridFull Time
5+ YOEBachelor's degree in science,3+ years promotional regulatory or OPDP/APLB experience,5+ years industry experience,knowledge of FDA promotional regulations,drug development and labeling processes.
AZAP
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
4d
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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
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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
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