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Systems Engineer L1 Jobs (NOW HIRING)

Transdev

Test Engineer L1

Atwater, CA · On-site

$104K - $120K/yr

The Systems Test Engineer shall be responsible for the evaluation of systems and or features, as well as developing and maintaining evaluation methods. Systems Test Engineers will manage and execute ...

Technium

Network Operations Engineer L1

Marlborough, MA · Remote

An Operations Engineer L1 is a highly motivated, technically savvy individual working in a Network and Security Operations Center. This position will require a proactive engineer who works well in a ...

Transdev

Test Engineer L1

Atwater, CA · On-site

$104K - $120K/yr

The Systems Test Engineer shall be responsible for the evaluation of systems and or features, as well as developing and maintaining evaluation methods. Systems Test Engineers will manage and execute ...

CycloKinetics

Chemical Engineer L1

Salt Lake City, UT · On-site

We are a team of engineers, scientists, and operators driven by performance, innovation, and ... The successful candidate must have theorical knowledge of catalytic systems, process integration ...

Service Global, Inc

Desktop Engineer L1

Irvine, CA · On-site

$22 - $23/hr

Good technical knowledge of Windows operating system (Windows 10 and 11) * Knowledge on Microsoft Office 2016 (Office 365) * Proven work experience as a Desktop Support Engineer, Technical Support ...

Cyngn, Inc.

Senior Systems Engineer

Mountain View, CA · On-site

$122K - $167K/yr

Translate L0/L1 product requirements and user stories into complete, unambiguous, and testable ... Act as the systems engineering point of contact for industrial safety certification, ensuring ...

Cyngn Inc.

Senior Systems Engineer

Mountain View, CA · On-site

$122K - $167K/yr

Translate L0/L1 product requirements and user stories into complete, unambiguous, and testable ... Act as the systems engineering point of contact for industrial safety certification, ensuring ...

Cognizant

Systems Engineer

New Albany, OH · On-site

Systems Engineer Job Location: Onsite- New Albany, OH, USA ** Please note, this role is not able to ... Lead and coordinate the day-to-day operations of L1 and L2 support teams by managing work ...

Power3 Solutions

Software Engineer L1

Laurel, MD · On-site

$100K - $175K/yr

Develops, maintains, and enhances complex and diverse software systems (e.g., processing- intensive ... Partnership with System Engineers to execute the agile process. * Prototyping of solution space in ...

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Systems Engineer L1 information

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$53.5K

$127.2K

$167K

How much do systems engineer l1 jobs pay per year?

As of Sep 13, 2026, the average yearly pay for systems engineer l1 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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For Systems Engineer L1 jobs, the most frequently searched job titles are:

Engineer - Quality L1

Dayville, CT • On-site

Putnam Plastics Corporation
Medical Equipment and Supplies Manufacturing • 201 - 500 employees
Learn more about Putnam Plastics Corporationexternal

$70K - $91K/yr

Full-time

Re-posted 7 days ago

Key responsibilities

  • Develops and maintains quality standards, plans, and procedures to ensure products and processes meet specifications, regulatory standards, and system requirements.

  • Investigates customer complaints, performs root cause analysis, and implements changes to the quality system as needed.

  • Participates in audits, supports internal and external compliance activities, and tracks quality and compliance-related activities.

Job description

Putnam Plastics Corporation (PPC) is the industry leading manufacture of life-saving medical devices components for over 40 years. We are looking for people who want to invest in their future, the future of PPC and our PPC community. Please refer to our website at putnamplastics.com/about/career-opportunities for more information.
This is a summary only. We are an EEO employer.
The Quality Engineer L1, in support of production, supplier quality, and development programs, is responsible for developing and maintaining quality standards, plans, and procedures to assure our products and processes meet required specifications, regulatory standards, and system requirements. A dedication to both company and departmental continuous improvement is required. Position includes cross functional team participation.
Essential Duties amp; Responsibilities:
  • Performs a wide variety of activities to ensure compliance with applicable quality objectives and regulatory requirements.
  • Investigates customer complaints, performs return sample evaluations, root cause analysis, and implements changes to the quality system when needed upon investigation communicate final reports to the customer.
  • Evaluates verification and validation protocols and reports to ensure compliance to external standards and internal standards and procedures.
  • Participates and leads CAPA'S as needed.
  • Evaluates RISK during reviews of non-conforming's.
  • Responsible for and facilitates the development and implementation of quality engineer metrics as KPIs. (Key Performance Indicators).
  • Review and approves controlled documents to ensure defined quality objectives are met.
  • Assist in the implementation and further development of quality and regulatory policies and procedures.
  • Tracks reoccurring quality and compliance-related activates with Supplier Quality.
Audits:
  • Participates in audits, customer meetings, support internal audits within the organization and tracks compliance of corporate QMS to applicable standards.
  • Knowledge base remains current of existing and emerging regulations, standards, or guidance documents including Medical Device Regulation (MDR) and all other standards /regulations including within scope as they pertain to training.
Required Qualifications:
  • Bachelor's degree in engineering or science, or equivalent work experience.
  • A minimum of two (2) years related to manufacturing experience in a QMS environment.
  • Working knowledge ISO 13485:2016 and FDA requirements (21 CFR 820) and other equivalent applicable standards.
  • Prior experience within electronic Quality Management Systems (eQMS) such as ETQ, Green Light Guru, Master Control, Qualio, Veeva, or similar applications and systems, as well as Minitab or other Statistical Programs.
  • Knowledge of Quality Assurance methods, such as process validations, statistical process control, design of experiments, and protocol/report writing.
Preferred Qualifications:
  • Bachelor's Degree in a technical field: plastics, mechanical, chemical, or biomedical engineer field and at least 5 years of relevant experience OR the equivalent combination of education.
  • At least 5 years of direct experience in a medical device company or similarly regulated environment with related Supplier Quality Engineer experience in a medical device or Pharma Company.
  • Working knowledge of Quality KPI and SPC.
  • Certification in training methods or ASQ Certifications such as Quality Engineer or Quality Auditor.
This is a summary only.

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