Killingly Center • 50 milesRemote · Hybrid · Onsite · Field · All Environments
Killingly Center • 50 milesRemote · Hybrid · Onsite · Field · All Environments
Killingly Center • 50 milesRemote · Hybrid · Onsite · Field · All Environments
Killingly Center • 50 milesRemote · Hybrid · Onsite · Field · All Environments
14 clinical engineer jobs at 11 companies in Killingly Center, CT
1mo
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Clinical Specialist II
Hartford or United States
$61k-$123k/yr RemoteFull Time
2+ YOEBachelor's in biomedical engineering or equivalent healthcare experience; ability to be certified on EP products; minimum 2 years clinical experience and 6+ months in a Clinical Specialist role; primary mapping experience and sales activities required; vendor credentialing (may include COVID-19 vaccination).
EP products, Abbott Advanced Mapping and Ablation Tools
1mo
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Clinical Specialist II
Hartford, Connecticut, United States
$61k-$123k/yr RemoteFull Time
2+ YOEBachelor’s in biomedical engineering or related (or equivalent healthcare experience); ability to be certified on EP products; minimum 6 months in Clinical Specialist role and 2 years clinical experience; primary mapper experience and case-volume requirements; vendor credentialing (may include COVID-19 vaccination).
EP products, Advanced Mapping and Ablation Tools
3mo
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Lead Bioinformatics Engineer (Hyrbid)
Marlborough, Massachusetts, United States
$155k-$175k/yr HybridFull Time
7+ YOEBS with 7+ yrs, MS with 4+ yrs, or PhD with 3+ yrs in clinical/biological data; 5+ yrs in regulated life sciences; 4+ yrs software/engineering.
Python, JavaScript, TypeScript, R, Terraform, AWS CDK, Docker, Git, GitLab CI/CD, GitHub CI/CD, Flask, React, Bootstrap, Jupyter, R Markdown, ggplot2, tidyverse, Plotly, matplotlib, Tableau, d3.js
1w
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Principal Clinical Quality Assurance Specialist
Marlborough, Massachusetts, United States
$117k-$222k/yr HybridFull Time
5+ YOEBachelor's degree in science/engineering/health-related field, 5+ years clinical QA or clinical research compliance experience, 5+ years conducting GCP/regulatory audits, knowledge of ISO 14155/13485/GCP/GMP/GDP, CAPA and quality systems experience.
2mo
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Corporate Quality and Clinical Auditor
Marlborough or Newark
$138k-$230k/yr OnsiteFull Time
8+ YOEB.S. in engineering or science required; active auditor certifications preferred; 8+ years in quality/R&D/compliance and 5+ years as clinical/lead auditor; strong regulatory knowledge and audit, validation, and statistical skills.
Microsoft SharePoint, Microsoft Teams, Microsoft PowerPoint, Microsoft Excel
4w
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Principal Signal Processing Engineer - Cardiac Ablation Solutions
Newton, Massachusetts, United States
$153k-$229k/yr OnsiteFull Time
7+ YOEDevelop and validate real-time high-performance signal processing algorithms and production software for cardiac ablation devices; experience in DSP, algorithm verification, and clinical data analysis required.
Python, C++, Linux
4w
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Principal Signal Processing Engineer - Cardiac Ablation Solutions
Newton, Massachusetts, United States
$153k-$229k/yr OnsiteFull Time
3+ YOEAdvanced signal processing experience designing and implementing high-performance production code; 5+ years typical; proficiency in Python, C++, Linux; experience with ML, verification/validation, and clinical data analysis.
Python, C++, Linux
1d
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Lead Computer Systems Validation Engineer I (Clinical & R&D)
Waltham, Massachusetts, United States
$110k-$126k/yr HybridFull Time
7+ YOEBachelor’s degree in computer science, life sciences, engineering, or related field with 9+ years in digital quality; master’s with 7+ years considered. Requires GxP, CSV, quality systems, compliance, data integrity, and team leadership experience.
Learning Management System (LMS), Veeva DMS, TrackWise, TrackWise Digital, ValGenesis, GAMP 5, Artificial Intelligence (AI), Quality Risk Management, Change Control, CAPAs, SOPs
1mo
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THCE Clinical Engineering Manager
Hartford, Connecticut, United States
$98k-$147k/yr OnsiteFull Time
5+ YOEAssociate in biomedical or related field plus 5+ years hospital service leadership or equivalent; medical equipment service and project management experience; MS Office skills; leadership, analytical, and budgeting abilities; occasional travel.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint
2mo
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Clinical Engineering Technician II
Middletown, Connecticut, United States
OnsiteFull Time
5+ YOEPerform preventive and corrective maintenance, safety testing, and repairs on medical equipment; CBET required; 5 years experience repairing medical equipment; adept with test equipment and documenting work in a computer management system.
1mo
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Lead Bioinformatics Engineer
Marlborough or Addison or Secaucus
$155k-$175k/yr RemoteFull Time
3+ YOEBS+7 / MS+4 / PhD+3 experience with clinical/biological data, 5+ years in regulated life sciences, 4+ years software development, cloud (AWS) and bioinformatics experience, programming in Python/JavaScript/R, SQL/NoSQL, Terraform, Docker.
SQL, NoSQL, JSON based RESTful APIs, AWS, Terraform, AWS CDK, Microsoft Visio, DrawIO, Python, javascript/typescript, R, Docker, Python Flask, React Native, Bootstrap, R Markdown, Jupyter Notebook, ggplot2, tidyverse, Plotly, matplot lib, Tableau, d3.js, Git, Gitlab CI/CD, Github CI/CD
2mo
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Adjunct Instructor in Generative AI in Clinical Decision Support
Waltham, Massachusetts, United States
RemotePart Time
3+ YOEAdvanced degree (Masters or Ph.D.) in Computer Science, Health Informatics, Data Science, Engineering or related field; strong AI healthcare knowledge; 3+ years AI deployment experience; programming in Python or R; online teaching experience; strong online communication.
Python, R, Moodle
3w
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VP of Operations
Needham, Massachusetts, United States
OnsiteFull Time
10+ YOESenior operating leader to run day-to-day operations, own finance and metrics, build scalable systems, design org and hiring, and partner across clinical, data, product, and engineering.
2mo
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Post Market Surveillance SME - Medical Device #6887
Marlborough, Massachusetts, United States
OnsiteFull Time, Contract
5+ YOEBachelor's in engineering/life sciences/quality/regulatory required, 5+ years in medical device quality/regulatory/clinical/post-market surveillance, strong knowledge of FDA, EU MDR, ISO 13485/14971, complaint/CAPA/risk management, analytical and technical writing skills. Must be authorized to work in the U.S. without sponsorship.