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Contract Embedded Systems Engineer Jobs in Delaware

System Engineer Location: Newark, DE Long Term Contract Job Overview: We are seeking highly skilled and experienced System Engineers to join our team. The ideal candidate will have 5-8 years of ...

QA Test Automation Engineer Location: Dover, DE (Onsite) Duration: 6+ months Interview process: 2 ... Experience testing robotics, embedded systems, or hardware-integrated software * Experience with CI ...

Quality Engineer

Newark, DE · On-site

$70K - $90K/yr

Position Summary Qnity Electronics is seeking a Quality Systems Engineer to serve as a key leader ... is embedded in everything we do. This position is 100% onsite in our Newark, Delaware facility.

Job Purpose The Application Security Engineer is responsible for strengthening the security of our ... Experience securing embedded systems and mobile applications. Reasoning Ability Problem management ...

Senior Hardware Engineer

Wilmington, DE

$107K - $143K/yr

Competence in robotics engineering, including mechanical engineering, PCB design, and embedded systems; * Track-record in robot design, prototyping, testing, and producing quality documentation for ...

$122K - $161K/yr

Joyson Safety Systems harnesses collaboration and innovation to ensure quality and exemplary ... Integrate algorithms into embedded architectures, supporting optimization, performance tradeoff ...

Showing results 21-40

Contract Embedded Systems Engineer information

What is a contract embedded systems engineer?

Contract Embedded Systems Engineers are professionals hired on a temporary or project basis to design, develop, and maintain embedded systems—specialized computing systems that perform dedicated functions within larger mechanical or electrical systems. Unlike permanent employees, contract engineers typically work for a set period or until a specific project is completed, offering flexibility to both engineers and employers. They may work on projects involving hardware and software integration, firmware development, real-time operating systems, and troubleshooting embedded devices. Their skills are often sought in industries like automotive, consumer electronics, medical devices, and industrial automation.

What are the key skills and qualifications needed to thrive as a contract embedded systems engineer?

To thrive as a Contract Embedded Systems Engineer, you generally need a solid background in computer engineering or electrical engineering, with expertise in C/C++ programming, real-time operating systems (RTOS), and hardware-software integration. Familiarity with tools like oscilloscopes, logic analyzers, version control systems (such as Git), and protocols like SPI, I2C, or UART is typically required, along with certifications like Certified Embedded Systems Engineer (CESE) being advantageous. Strong problem-solving skills, adaptability, and effective communication are crucial soft skills for collaborating with diverse teams and clients. These skills and qualifications are essential to deliver reliable, efficient embedded solutions on time while meeting client specifications in a dynamic contract environment.

What are some common challenges faced by contract embedded systems engineers, and how can they be addressed?

Contract embedded systems engineers often encounter challenges such as rapidly adapting to new codebases, working within tight project timelines, and ensuring seamless integration with existing hardware and software. Success in this role often requires strong communication with both in-house and external teams to clarify requirements and resolve issues quickly. Proactively documenting your work, asking clarifying questions early, and leveraging version control systems can help manage these challenges and deliver reliable solutions on schedule.

What is the difference between Contract Embedded Systems Engineer vs Contract Firmware Engineer?

AspectContract Embedded Systems EngineerContract Firmware Engineer
Required CredentialsBachelor's in Electrical, Computer Engineering, or related; often certifications in embedded systemsBachelor's in Computer Science, Electrical Engineering; certifications in embedded or firmware development
Work EnvironmentDesigning and testing embedded hardware/software in labs or on-siteDeveloping and debugging firmware primarily in software environments
Employer & Industry UsageElectronics, aerospace, automotive, industrial automationConsumer electronics, IoT devices, robotics, embedded systems

Contract Embedded Systems Engineers focus on designing and integrating hardware and software for embedded systems, often working with both hardware and firmware. Contract Firmware Engineers specialize in developing low-level software that runs directly on embedded hardware. While both roles require embedded systems knowledge, the embedded systems engineer has a broader scope including hardware design, whereas firmware engineers concentrate on software development within embedded environments.

What are the most commonly searched types of Embedded Systems Engineer jobs in Delaware?

The most popular types of Embedded Systems Engineer jobs in Delaware are:

What are popular job titles related to Contract Embedded Systems Engineer jobs in Delaware?

For Contract Embedded Systems Engineer jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Contract Embedded Systems Engineer jobs in Delaware look for?

The top searched job categories for Contract Embedded Systems Engineer jobs in Delaware are:

What cities in Delaware are hiring for Contract Embedded Systems Engineer jobs?

Cities in Delaware with the most Contract Embedded Systems Engineer job openings:

System Engineers

Fusion Life Sciences

Newark, DE • On-site

Contractor

Re-posted 13 days ago


Job description

Title: System Engineer

Location: Newark, DE

Long Term Contract
 

Job Overview:

We are seeking highly skilled and experienced System Engineers to join our team. The ideal candidate will have 5-8 years of experience in the medical device industry, with a strong focus on Design Controls, traceability, and design validation. This individual will play a critical role in ensuring that user needs are clearly traced to design inputs, verification, and validation throughout the product development lifecycle.

Key Responsibilities:

  • Design Controls: Lead efforts to develop and implement robust design control processes for new and existing products, ensuring compliance with FDA regulations (21 CFR 820), ISO 13485, and other relevant industry standards.
  • Traceability: Establish and maintain traceability throughout the design and development phases, ensuring that user needs, design inputs, and verification requirements are fully traced and documented.
  • User Needs to Design Validation: Work cross-functionally to trace user needs to design validation, ensuring that final products meet both the defined requirements and user expectations. This includes the development of comprehensive Design History Files (DHF) and validation documentation.
  • Design Verification & Validation (V&V): Collaborate with teams to ensure that all products undergo thorough design verification and design validation processes, providing evidence that the product meets the necessary specifications.
  • Cross-Functional Collaboration: Work closely with other engineering disciplines, such as hardware, software, and quality teams, to ensure a seamless integration of design controls and traceability throughout the product lifecycle.
  • Documentation and Reporting: Prepare and maintain detailed documentation for design control processes, ensuring all deliverables are compliant with internal and regulatory standards. Provide updates to leadership and stakeholders on project status, risks, and timelines.
  • Continuous Improvement: Identify areas for process improvements in design control and traceability methods, and implement changes that enhance the efficiency and effectiveness of product development.

Required Qualifications:

  • Experience: 5-8 years of experience in system engineering within a regulated environment, preferably in medical devices or other highly regulated industries.
  • Design Controls: Strong experience in implementing and managing design controls processes, including traceability, user needs, and design verification/validation.
  • Traceability: Proven ability to ensure full traceability from user needs to design validation and manage product documentation accordingly.
  • Regulatory Knowledge: In-depth knowledge of FDA regulations (21 CFR 820), ISO 13485, and other applicable standards for medical devices.
  • Collaboration: Strong communication and interpersonal skills, with experience working effectively in cross-functional teams.
  • Strong verbal and written communication in English

Preferred Qualifications:

  • Risk Management: Experience with risk management processes, including risk analysis, risk assessment, and mitigation strategies (e.g., ISO 14971).
  • V&V Experience: Familiarity with verification and validation techniques and methodologies for ensuring that product designs meet both functional and regulatory requirements.
  • Software and Tools: Experience with requirements management tools, traceability software, and common V&V tools.

Personal Attributes:

  • Strong analytical and problem-solving skills
  • Ability to manage and prioritize multiple tasks in a fast-paced environment
  • Detail-oriented with a commitment to accuracy
  • Proactive and able to work independently or as part of a team
     
    Sincerely,
    Subash Kondala
    Medical/Pharma Recruiter
    www.fusionlifesolutions.com 
    Subash@fusionlifesolutions.com
    Direct Number: (312)447-9550
    linkedin.com/in/subash-kondala-a5a39424a
    For all jobs with Fusion https://tinyurl.com/56f356a3
    6110 McFarland Station Dr Suite 502 Alpharetta GA 30004