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System Engineers Jobs (NOW HIRING)

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 ...

System Engineer

San Jose, CA · On-site

$85K - $100K/yr

We seek talented, passionate, and committed engineers, technologists, and business leaders to join us. Job Summary: High-performance server product team in Supermicro is seeking talented System ...

System Engineer

San Jose, CA · On-site

$85K - $100K/yr

We seek talented, passionate, and committed engineers, technologists, and business leaders to join us. Job Summary: High-performance server product team in Supermicro is seeking talented System ...

System Engineer

Laurel, MD · On-site

$115K - $165K/yr

Our team consists of System Engineers, Software Engineers, Test Engineers, and Signals Analysts performing work throughout the Continental United States (CONUS) and Outside the Continental United ...

System Engineer

San Jose, CA · On-site

$85K - $100K/yr

We seek talented, passionate, and committed engineers, technologists, and business leaders to join us. Job Summary: High-performance server product team in Supermicro is seeking talented System ...

System Engineer

San Jose, CA · On-site

$90K - $110K/yr

We seek talented, passionate, and committed engineers, technologists, and business leaders to join us. Job Summary: High-performance server product team in Supermicro is seeking talented System ...

Summary CTC Group is seeking System Engineers for a contingent program to perform systems engineering functions, including defining and documenting concept of operations, operational/system ...

Sr. System Engineer

San Jose, CA · On-site

$137K - $156K/yr

We seek talented, passionate, and committed engineers, technologists, and business leaders to join us. Job Summary: High-performance product team in Supermicro is seeking talented Sr. System Engineer ...

Ability to work with large teams of distributed ground system engineers and senior level engineers of multiple disciplines. * Good interpersonal and leadership skills. * A willingness and ability to ...

Ability to work with large teams of distributed ground system engineers and senior level engineers of multiple disciplines. * Good interpersonal and leadership skills. * A willingness and ability to ...

Provide guidance and mentorship to junior system engineers and other team members, fostering a culture of continuous learning and professional growth. * Stay up-to-date with industry trends, emerging ...

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System Engineers information

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$53.5K

$127.2K

$167K

How much do system engineers jobs pay per year?

As of Aug 12, 2026, the average yearly pay for system engineers in the United States is $127,215.00, according to ZipRecruiter salary data. Most workers in this role earn between $98,000.00 and $157,000.00 per year, depending on experience, location, and employer.
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What cities are hiring for System Engineers jobs? Cities with the most System Engineers job openings:
What states have the most System Engineers jobs? States with the most job openings for System Engineers jobs include:
Infographic showing various System Engineers job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $127,215 per year, or $61.2 per hour.

System Engineers

Fusion Life Sciences

Newark, DE • On-site

Contractor

Re-posted yesterday


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