10 medical device manager engineering jobs at 6 companies in Miami, FL
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Senior Device Engineer
Coral Springs, Florida, United States
OnsiteFull Time
5+ YOEBachelor's in engineering and 5+ years device or medical product experience; expertise in device design, reliability testing, regulatory standards (ISO/ASTM/ICH), FMEA/Human Factors, and SolidWorks/CAD tools.
SolidWorks, CAD
2w
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Director, Engineering
Sunrise, Florida, United States
$169k-$236k/yr OnsiteFull Time
10+ YOE7+ MgmtBS in engineering, 10+ years in medical device or regulated manufacturing, 7+ years leading engineering teams, experience with DFSS/DFM/DFA and Lean Six Sigma, strong leadership, project management, and regulatory knowledge.
2w
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Manufacturing Engineer II (TAS)
Sunrise, Florida, United States
OnsiteFull Time
5+ YOEBachelor's in engineering,5+ years medical device technical experience,project management experience,hands-on tooling and process development skills,ability to run experiments and root cause investigations.
AutoCAD, SolidWorks
2w
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Manufacturing Engineer I (TAS)
Sunrise, Florida, United States
OnsiteFull Time
3+ YOEBachelor's in engineering or equivalent, 3+ years medical device technical experience, project management, hands-on manufacturing knowledge, QMS/design control familiarity, strong communication and problem-solving.
SAP/HANA, AutoCAD, SolidWorks
2w
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Manufacturing Engineer II (TAS)
Sunrise, Florida, United States
OnsiteFull Time
5+ YOEBachelor's in engineering or equivalent, 5+ years in medical device technical roles, project management, hands-on tooling/process and prototyping, knowledge of electronics, polymers, metals and packaging, QMS and safety awareness.
AutoCAD, SolidWorks
3w
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Engineer I, Product Development
Miami, Florida, United States
$69k-$86k/yr OnsiteFull Time
1+ YOEBachelor's in engineering,1+ years medical device/biotech experience,knowledge of cGMP/design controls and risk management,experience with V&V and technical writing,strong data analysis and problem-solving skills.
Minitab, SPSS
2mo
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Commissioning and Qualification Engineer
Tamarac or Miramar
$85k-$95k/yr OnsiteFull Time
2+ YOEBachelor's in engineering (Master's preferred), 2+ years commissioning and qualification experience in pharmaceutical/medical device, GMP/CFR/ICH knowledge, statistics/DoE, CAPA and project management, proficient with Word/Excel/Project/Minitab.
Microsoft Word, Microsoft Excel, Microsoft Project, Minitab
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Senior Regulatory Affairs Specialist-Hybrid Fort Lauderdale, FL
Fort Lauderdale, Florida, United States
HybridFull Time
5+ YOEB.S. in life sciences/engineering plus 5+ years regulatory affairs experience in medical device/IVD; post-market compliance, change management, and FDA submission exposure; strong technical writing and communication.
Microsoft Office, electronic document management systems
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Supervisor, Quality Control (TAS)
Sunrise, Florida, United States
$72k-$100k/yr OnsiteFull Time
5+ YOESupervise QC inspectors, analyze trends, manage non-conformances/CAPA, ensure compliance with ISO 13485 and 21 CFR Part 820, conduct audits, and support validations; BS in Engineering or 5+ years medical device quality experience preferred.
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Software Engineer III - C#, Digital Pathology Image Management System development
Miami, Florida, United States
$120k-$135k/yr HybridFull Time
5+ YOE5+ years software development experience; Bachelor's in a relevant scientific or engineering discipline (or equivalent); expertise in C#, Microsoft .NET Framework 4.8/.NET Core, ASP.NET, REST APIs, frontend (CSS, JavaScript, React), Node.js, databases (PostgreSQL, SQLite), version control/tools (JIRA, Bitbucket, Git); experience with digital slide ...
C#, Microsoft .NET Framework 4.8, Microsoft .NET Core 2.0, CSS, JavaScript, Microsoft WPF, Microsoft WinForms, MVC, Microsoft ASP.NET, REST API, PostgreSQL, SQLite, JIRA, Bitbucket, Git, C++, Node.js, React, DICOM, TIFF, SVS, MRXS, iSyntax, NDPI, HL7, SNOMED, IEC 62304, ISO 14971, ISO 13485, FDA Requirements