348 fda jobs at 152 companies in Cherry Hill, NJ
3mo
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Director, Manufacturing Quality, GIS (Japan Based) (Center Valley, PA, US, 18034-0610)
Center Valley or Aizu
$135k-$189k/yr OnsiteFull Time
10+ YOE10+ years quality experience in regulated environment; FDA QSR/ISO 13485 knowledge; ASQ preferred; must relocate for Japan assignment.
FDA QSR, ISO 13485, MDR, CAPA, DHF, DMR, DHR
5d
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Quality & Compliance Manager
New Britain or Exeter or Seabrook
OnsiteFull Time
5+ YOERequires 5+ years in senior medical device or pharmaceutical quality assurance, FDA or Notified Body inspection experience, people management, advanced Microsoft Office, and fluent English.
Microsoft Office, FDA, ISO 13485
6d
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Study Director
South Brunswick Township or Dayton
$70k-$100k/yr OnsiteFull Time
5+ YOEBachelor's degree in a related field, 5+ years overseeing biocompatibility studies, knowledge of EPA, FDA, DOT, OECD, GLP, and ISO regulations, leadership, administration, communication, and writing skills.
EPA, FDA, DOT, OECD, GLP, ISO
3w
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Packaging Engineer
Summit or Fort Washington
$71k-$107k/yr OnsiteFull Time
5+ YOERequires 5–7 years of professional experience; bachelor's degree in packaging engineering preferred. Experience with packaging validation, specifications, component development, skin care or cosmetics, FDA, or GMP preferred.
FDA, GMP
1w
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Plant Engineer
Macungie, Pennsylvania, United States
OnsiteFull Time
3+ YOEBachelor's degree in mechanical, chemical, or electrical engineering with 3–5 years of related experience; requires manufacturing troubleshooting, project management, FDA/cGMP knowledge, AutoCAD, and strong communication skills.
AutoCAD, SolidWorks, FDA, cGMP, URS, FRS, FAT, SAT
3d
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President and General Manager, Interventional
Wayne, Pennsylvania, United States
OnsiteFull Time
15+ YOEBachelor’s degree and 15 years in medical devices with increasing responsibility and commercial experience. Requires interventional market expertise, Class 3 PMA experience, clinical trials, FDA panels, and CMS reimbursement knowledge.
R&D, P&L, FDA, CMS, Global Supply Chain (GSC), Quality Assurance and Regulatory Affairs (QARA)
14h
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Refining Operator - Weekend Night Shift - $23/hr +$5 Shift Differential
East Greenville, Pennsylvania, United States
$23/hr OnsiteFull Time
High school diploma or equivalent preferred; ability to operate and adjust machinery, perform quality checks, handle materials up to 50 pounds, and follow OSHA, GMP, FDA HACCP, and allergen management requirements.
FDA, HACCP, OSHA, GMP
3w
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Principal Scientist
Cherry Hill, New Jersey, United States
$118k-$135k/yr OnsiteFull Time
10+ YOEBS in Chemistry (advanced degree preferred), 10+ years pharmaceutical/analytical lab experience, method development/validation leadership, expertise in HPLC/UPLC/GC/dissolution/UV/FTIR and cGMP/ALCOA+/FDA/ICH/USP/EP, strong technical writing and communication.
HPLC, UPLC, GC, Dissolution, UV, FTIR, cGMP, ALCOA+, FDA, ICH, USP, EP
1mo
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Associate Director, REMS Operations (68770)
Parsippany or West Chester or United States
$159k-$194k/yr HybridFull Time
7+ YOEBachelor's degree, 7+ years program/project management in regulated industry (preferably pharma), 2+ years working with FDA, vendor management, FDA/REMS regulatory expertise, MS365 skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, MS Project, MS365, database
3mo
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Assistant Quality Unit Manager
Gibbstown, New Jersey, United States
$70k-$90k/yr OnsiteFull Time
5+ YOEMinimum 5 years’ related experience; knowledge of FDA CFR 210/211, cGMP Pharma; FDA CFR 820 / ISO 13485 cGMP Medical Device;Bachelor’s in technical/science.
ERP/MRP, QMS
2d
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Associate Director/Director, Regulatory Affairs Advertising & Promotions
Monmouth Junction, New Jersey, United States
$160k-$230k/yr HybridFull Time
3+ YOERequires a life sciences, pharmacy, or medicine degree; 3–8 years of promotional regulatory review experience depending on level; FDA advertising regulations expertise and direct FDA OPDP experience.
Food and Drug Administration (FDA), Office of Prescription Drug Promotion (OPDP), Form FDA-2253
4w
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Risk Management Associate I
Malvern, Pennsylvania, United States
$75k-$85k/yr OnsiteFull Time
4+ YOEBachelor's in life sciences, 4+ years in FDA-regulated industry with quality/regulatory compliance experience; knowledge of ISO 13485/14971 and FDA QSR; strong communication, leadership, project and database skills.
1mo
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Associate Director, REMS Operations
Parsippany or West Chester
$159k-$194k/yr HybridFull Time
7+ YOE2+ MgmtBachelor's degree, 7+ years program/project experience in regulated industry (pharma preferred), 2+ years interacting with FDA, vendor and budget management, FDA regulatory knowledge, MS Office and project tools proficiency, leadership experience.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project, Microsoft 365
2w
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Director, Operations
Cherry Hill, New Jersey, United States
OnsiteFull Time
8+ YOEBS in engineering or life sciences required (MS/MBA preferred); 8+ years FDA-regulated pharmaceutical manufacturing experience, sterile injectable experience preferred; strong cGMP, FDA inspection, aseptic process, leadership, budgeting, and continuous improvement skills.
Lean, Six Sigma
2mo
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Associate Director, Regulatory Affairs - Biosimilars (US)
Princeton, New Jersey, United States
$146k-$279k/yr HybridFull Time
7+ YOE7+ years regulatory affairs in biopharma with US biosimilar experience; FDA submissions; strong cross-functional leadership and communication.
1w
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Quality Engineer II
Quakertown, Pennsylvania, United States
OnsitePart Time
3+ YOEBachelor's in engineering or 3+ years relevant experience; knowledge of QMS, FDA and international regulations, process validation, CAPA and Microsoft Office.
Microsoft Office
2mo
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Director--Operations
Audubon, Pennsylvania, United States
OnsiteFull Time
10+ YOE10+ MgmtBachelor’s in Life Sciences or Engineering; 10+ yrs supervisory/production exp; strong leadership; FDA experience; CI/OEE focus.
ERP systems, Opex
3mo
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Medical Oncologist / Principal Investigator
East Brunswick, New Jersey, United States
OnsiteFull Time
MD with board certification in hematology and/or medical oncology; clinical trials experience; knowledge of GCP, FDA regulations; strong collaboration and communication skills.
4w
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International Regulatory Specialist
Audubon, Pennsylvania, United States
OnsiteFull Time
5+ YOEBachelor's in engineering or science,5 years related experience,experience with US FDA and international regulatory requirements and EU MDR technical documentation.
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 or Life Sciences; 7–10 years regulatory affairs; US FDA; OTC monograph; strong communication and project leadership.
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