1

System Validation Engineer Jobs (NOW HIRING)

This is an excellent opportunity for professionals with experience in validation, quality systems ... Engineering or related field (Master's preferred) • 2-3+ years of Validation Engineering ...

Perform process, equipment, system, and software validation activities. * Review and assess change ... Mentor junior engineers and provide technical guidance when required. Required Qualifications:

Seeking a Senior Validation Engineer with strong GMP experience to support QC equipment validation and Computer System Validation (CSV) activities. Key Responsibilities: * Author & execute URS, IQ/OQ ...

The Validation Engineer will be responsible for the following. * Develop, approve, and execute ... Design and develop manufacturing control systems in support of process operations. * Interact with ...

Validation Engineer | Walker, MI Salary Range: $81,000 - $121,000 depending on experience Are you a ... Perform risk assessments and generate validation plans for new and modified systems. * Analyze data ...

next page

Showing results 1-20

System Validation Engineer information

See salary details

$29

$51

$75

How much do system validation engineer jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for system validation engineer in the United States is $51.80, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $64.42 per hour, depending on experience, location, and employer.

How does a System Validation Engineer typically collaborate with cross-functional teams during the product development cycle?

System Validation Engineers frequently work closely with design, firmware, hardware, and software teams to ensure products meet specifications and function as intended. They participate in planning meetings, provide feedback on testability, and share validation results to help resolve issues quickly. Effective collaboration is essential, as validation often uncovers problems that require prompt cross-team coordination to address. This collaborative environment fosters continuous learning and a strong understanding of the entire product lifecycle.

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

To thrive as a System Validation Engineer, you need a solid background in electronics, computer engineering, or a related field, along with experience in hardware and software validation processes. Familiarity with tools like oscilloscopes, logic analyzers, scripting languages (e.g., Python), and test automation frameworks is typically required. Strong analytical thinking, problem-solving abilities, and clear communication help differentiate top performers in this role. These skills and qualities are crucial for ensuring that systems meet performance, reliability, and quality standards before reaching customers.

What does a System Validation Engineer do?

A System Validation Engineer is responsible for ensuring that electronic systems and products function as intended by systematically testing and validating hardware and software components. They design and execute test plans, analyze results, and collaborate with design and development teams to identify and resolve issues. Their work helps guarantee product reliability, performance, and compliance with industry standards before release to customers.
More about System Validation Engineer jobs
What cities are hiring for System Validation Engineer jobs? Cities with the most System Validation Engineer job openings:
Who are the top companies hiring for System Validation Engineer jobs? The top employers for System Validation Engineer jobs are:
What states have the most System Validation Engineer jobs? States with the most job openings for System Validation Engineer jobs include:
Computer System Validation Engineer

Computer System Validation Engineer

Avid Bioservices

Tustin, CA • On-site

$82K - $104K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 3 days ago


Job description

Description
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The Computer System Validation Engineer is responsible for providing technical validation support for manufacturing equipment, laboratory instruments, computer systems, networks, and software that have been newly installed, upgraded, replaced and/or modified in the cGMP Manufacturing Facility as well as its related manufacturing support areas, which may include Facilities/ Engineering, Quality Assurance, Supply Chain, and Quality Control.
  • Review and help author User Requirement Specification (URS) and/or Requirement Specification documents for manufacturing equipment/systems and processes
  • Generate and execute Installation, Operational and Performance/Process qualification (IQ, OQ, PQ) protocols, engineering studies and final reports that comply with corporate and regulatory requirements.
  • Coordinate and oversee validation protocol execution or validation activities with cross-functional departments.
  • Evaluate and analyze qualification data collected during projects, while verifying acceptability of the data and compliance with the approved protocol.
  • Ensure any deviations to protocols and/or deviations to acceptance criteria are adequately addressed, documented and reviewed by the Validation Committee
  • Provide input and assist on the development of validation policies and procedures.
  • Effectively interact and provide validation guidance to other departments.
  • Assist department manager in developing realistic time and resource requirements for validation activities in support of company expectation.
  • Provide input and assist in change control assessment and Part 11 assessment for validated systems.
  • Review Standard Operating Procedures (SOPs) and ensure the operational parameters described in the SOP for the equipment reflects validated conditions.
  • Assist department manager on other types of projects/managerial responsibilities as needed

Minimum Qualifications:
  • BA/BS in science (such as Biology, Microbiology, Biochemistry, Chemistry), Engineering (such as Electrical, Electronics, Computer Science) or other equivalent technology related field.
  • Minimum of 3 years' work experience in biopharmaceutical/pharmaceutical manufacturing environment of which 1 year is directly involved in validations.

Position Type/Expected Hours of Work:
This role is a full-time position. Days and hours of work are Monday through Friday, 8am to 5pm PST, unless otherwise stated by Supervisor.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $82,000- $104,400 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.