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Clinical Engineer Jobs in Delaware (NOW HIRING)

Our wide network of consultants and contract-to-hire engineers brings deep expertise across ... Clinical Scientist - Medical Devices Location: Newark, DE Long Term Contract Role: Clinical ...

Oncology/Solid Tumors Director, Clinical Research Scientist (CS) Contractor Scope of Services: This ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Clinical Director

Georgetown, DE · On-site

$95K - $105K/yr

Clinical Director Reports to: Chief Medical Officer Primary Location : Georgetown - (incumbent may ... Manage specialized programs including the 340B discount pharmacy and discount vaccine programming.

Systems Engineer

Newark, DE · On-site

$78K - $122K/yr

Develop an in-depth understanding of system architecture design and clinical use of medical imaging ... Support engineering teams and system quality assurance through concept, implementation, and ...

Systems Engineer

Newark, DE · On-site

$78K - $122K/yr

Develop an indepth understanding of system architecture design and clinical use of medical imaging ... Support engineering teams and system quality assurance through concept, implementation, and ...

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Clinical Engineer information

See Delaware salary details

$40.5K

$93.8K

$136.1K

How much do clinical engineer jobs pay per year?

As of Jun 9, 2026, the average yearly pay for clinical engineer in Delaware is $93,780.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,100.00 and $109,600.00 per year, depending on experience, location, and employer.

What does a Clinical Engineer do?

A Clinical Engineer is a professional who applies engineering principles to the healthcare field, particularly in medical technology and equipment management within hospitals and clinics. Their main responsibilities include ensuring the safe and effective use of medical devices, maintaining and troubleshooting equipment, and providing technical support to medical staff. Clinical Engineers may also be involved in equipment procurement, regulatory compliance, and training users on new technologies. By bridging the gap between engineering and medicine, they help improve patient care and safety.

What is the difference between Clinical Engineer vs Biomedical Equipment Technician?

AspectClinical EngineerBiomedical Equipment Technician
CredentialsBachelor's degree in engineering or related field; certifications like CBET or CCEAssociate's or bachelor's degree; certifications like CBET or CRES
Work EnvironmentDesign, evaluate, and oversee medical equipment; collaborate with healthcare staffMaintain, repair, and calibrate medical devices on-site in healthcare facilities
Employer & IndustryHospitals, medical device companies, healthcare institutionsHospitals, clinics, biomedical service companies

Clinical Engineers focus on the design, evaluation, and management of medical equipment, often working on system integration and safety protocols. Biomedical Equipment Technicians primarily handle the maintenance, repair, and calibration of medical devices. Both roles are essential in healthcare settings, but Clinical Engineers typically have a broader scope involving engineering principles and system oversight, while Biomedical Equipment Technicians focus on hands-on equipment servicing.

What Is a Clinical Engineer?

A clinical engineer collaborates with scientists to develop medical equipment and biomedical research advances. Testing and designing medical technology are their primary responsibilities. Your work may involve artificial tissues, such as joints, hearing implants, and heart valves; pharmaceuticals; medical instruments; or diagnostic equipment, like imaging machines and monitoring apparatus. Job duties include maintaining biomedical equipment and computer systems, overseeing teams of technicians, and leading research studies in biomedical technology.

How does a Clinical Engineer typically interact with clinical staff and medical device vendors in a healthcare setting?

Clinical Engineers play a pivotal role in bridging the gap between medical technology and clinical practice. They regularly collaborate with clinical staff to ensure that medical equipment is used safely and efficiently, providing training and addressing any technical concerns. Additionally, Clinical Engineers coordinate with device vendors for equipment maintenance, troubleshooting, and upgrades, often acting as the primary point of contact during installations or when evaluating new technologies. This collaborative environment requires strong communication skills and a proactive approach to problem-solving, making teamwork a central aspect of the role.

What are the key skills and qualifications needed to thrive as a Clinical Engineer, and why are they important?

To thrive as a Clinical Engineer, you need a strong background in biomedical engineering, electronics, and healthcare technology, typically supported by a relevant degree and sometimes professional certification (e.g., CCE). Familiarity with medical device regulations, hospital equipment management systems, and quality assurance tools is essential. Excellent problem-solving, communication, and teamwork skills help Clinical Engineers collaborate with medical staff and address complex technical issues. These abilities are critical for ensuring the safety, compliance, and optimal performance of medical devices in healthcare environments.
What are the most commonly searched types of Clinical Engineer jobs in Delaware? The most popular types of Clinical Engineer jobs in Delaware are:
What are popular job titles related to Clinical Engineer jobs in Delaware? For Clinical Engineer jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Clinical Engineer jobs in Delaware look for? The top searched job categories for Clinical Engineer jobs in Delaware are:

Clinical Scientist

Techtrueup

Newark, DE • Remote

Contractor

Posted 27 days ago


Job description

Company Description

Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE-certified Healthcare Staffing and Engineering Services provider supporting industries including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food & Beverage, and Automotive. We proudly partner with 120+ clients such as Johnson & Johnson, Haemonetics, Delta, Caterpillar, Artisan Chef, Baxter, and many more. Our wide network of consultants and contract-to-hire engineers brings deep expertise across Engineering, Technical, Administrative, Healthcare, Life Sciences, Blue Collar, Skilled Trades, IT, Software Development, Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software's enabling us to source and screen top talent within hours. This ensures rapid response times, high-quality matches, and virtually zero attrition.

Job Description

Job Title: Clinical Scientist - Medical Devices

Location: Newark, DE

Long Term Contract
Role:
Clinical Scientist responsible for developing Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER) to support CE Mark regulatory submissions for medical devices.
Key Responsibilities:

  • Develop and author CEP and CER for regulatory submissions.
  • Conduct systematic literature reviews and analyze clinical data for device safety and performance.
  • Collaborate with R&D, Engineering, Regulatory Affairs, and Post-Market teams to support clinical strategy.
  • Prepare clinical documentation such as Investigator Brochures, Clinical Study Protocols, and Clinical Study Reports (CSR).
  • Respond to regulatory authority questions related to clinical evidence.
  • Review risk documentation and product labeling based on clinical data.
  • Manage clinical documentation timelines and ensure compliance with EU MDR, GCP, and corporate SOPs.

Required Qualifications:

  • MD, PhD, or MS in a scientific field.
  • 5-8 years of medical writing or clinical evaluation experience.
  • Experience in CER/CEP writing, literature review, and regulatory documentation.
  • Strong analytical, technical writing, and cross-functional collaboration skills.

Preferred:

  • 2-4 years of CER writing experience in the medical device industry.
  • Knowledge of EU MDR and clinical evaluation processes.
Additional Information

All your information will be kept confidential according to EEO guidelines.