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Senior Validation Engineer Jobs in Georgetown, TX

ICU Medical

Senior Validation Engineer

Austin, TX · On-site

$110 - $150/hr

Position Summary Completes advanced validation projects with peer input and guidance from engineering and validation management.A specialist on complex technical and business matters. Work is highly ...

Posted today

Socket.dev

Sr. System/Test Validation Engineer

Austin, TX · On-site

$110 - $140/hr

Working at our manufacturing site, you will collaborate with cross-functional engineering teams and manufacturing partners to deliver scalable test strategies, automation, validation infrastructure ...

Posted today

jobr.pro

Senior Firmware Validation Engineer

Austin, TX · On-site

$120 - $150/hr

Job Summary We are seeking a Senior Firmware Validation Engineer to support validation and quality assurance for the rack-level firmware stack across Graphcore's ARM-based server platforms. This role ...

Graphcore

Senior Firmware Validation Engineer

Austin, TX · On-site

$118K - $156K/yr

Job Summary We are seeking a Senior Firmware Validation Engineer to support validation and quality assurance for the rack-level firmware stack across Graphcore's ARM-based server platforms. This role ...

Graphcore

Senior Firmware Validation Engineer

Austin, TX · On-site

$118K - $156K/yr

Job Summary We are seeking a Senior Firmware Validation Engineer to support validation and quality assurance for the rack-level firmware stack across Graphcore's ARM-based server platforms. This role ...

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Senior Validation Engineer information

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How much do senior validation engineer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for senior validation engineer in Georgetown, TX is $60.18, according to ZipRecruiter salary data. Most workers in this role earn between $48.03 and $68.37 per hour, depending on experience, location, and employer.

What does a senior validation engineer do?

A Senior Validation Engineer is responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They develop and execute validation protocols, analyze test data, and document results to confirm compliance with industry and company standards. Senior Validation Engineers often lead validation projects, collaborate with cross-functional teams, and mentor junior staff. Their work is critical in industries like pharmaceuticals, biotechnology, and manufacturing, where product safety and efficacy are essential.

What are the key skills and qualifications needed to thrive as a senior validation engineer, and why are they important?

To thrive as a Senior Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically supported by a relevant degree and experience in validation within regulated industries. Familiarity with validation protocols (IQ, OQ, PQ), statistical analysis tools, and systems like FDA 21 CFR Part 11 is crucial. Strong problem-solving, attention to detail, and effective communication skills help ensure successful project outcomes and cross-functional collaboration. These skills and qualifications are essential to maintain product quality, meet regulatory standards, and drive continuous improvement.

What are some typical challenges faced by senior validation engineers when leading validation projects?

Senior Validation Engineers often encounter challenges such as managing tight project timelines, ensuring compliance with evolving regulatory standards, and coordinating cross-functional teams. Balancing the needs of production, quality assurance, and regulatory affairs requires strong communication and project management skills. Additionally, troubleshooting unexpected validation failures and documenting results thoroughly are key aspects that demand both technical expertise and attention to detail.

What is the difference between Senior Validation Engineer vs Validation Specialist?

AspectSenior Validation EngineerValidation Specialist
CredentialsBachelor's or Master's in Engineering, Life Sciences, or related fields; often with certifications like GxP or CSVSimilar educational background; certifications like GxP or CSV are common
Work EnvironmentDesigns and oversees validation protocols in manufacturing, biotech, or pharmaceutical settingsExecutes validation tasks, tests, and documentation in similar environments
Employer & IndustryPharmaceutical, biotech, medical device companiesSame industries, often working under validation teams
Search & ComparisonOften compared for experience level and responsibilitiesCommonly searched together for validation roles

The main difference is that a Senior Validation Engineer typically leads validation projects, designs protocols, and oversees validation activities, while a Validation Specialist focuses on executing validation tests and documentation. Both roles require similar credentials and work in comparable environments, but the Senior Validation Engineer has more responsibility for planning and oversight.

What are popular job titles related to Senior Validation Engineer jobs in Georgetown, TX?

For Senior Validation Engineer jobs in Georgetown, TX, the most frequently searched job titles are:

What cities near Georgetown, TX are hiring for Senior Validation Engineer jobs?

Cities near Georgetown, TX with the most Senior Validation Engineer job openings:

Senior Validation Engineer jobs near you
Infographic showing various Senior Validation Engineer job openings in Georgetown, TX as of August 2026, with employment types broken down into 86% Full Time, 9% Part Time, and 5% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $125,177 per year, or $60.2 per hour.

Senior Validation Engineer

ICU Medical

Austin, TX • On-site

$110 - $150/hr

Other

Posted 15 hours ago

Posted today

ICU Medical rating

7.8

Company rating: 7.8 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

154th of 545 rated manufacturers

Job description

Position Summary

Completes advanced validation projects with peer input and guidance from engineering and validation management.A specialist on complex technical and business matters. Work is highly independent. May assume a team lead role for the work group. May also lead validation contract support and be responsible for tracking validation hours and budget.

Essential Duties & Responsibilities
  • Analyzes, plans, organizes and completes projects of a very complex nature. Develops scope and provides creative solutions. Plans, organizes and conducts technical projects. Consolidates results of design elements of major projects for purpose of design review. Integrates subsystems and components in total systems design. Develops specifications from customer requirements.
  • Receives general project direction. Responsible for project progress.
  • Prepares, reviews, and executes computerized system validation protocols per local procedures and Food and Drug Administration (FDA)regulations.
  • Decisions consistently affect multiple or critical projects in the business and may impact external relationships.
  • Serve as project coordinator or project manager for validation/qualification aspects of projects.
  • Delivers communications tailored to the needs of the receiver (managers, peers, customers) with appropriate frequency to maximize its utility and promote cross-functional collaboration. Brings substantive conflicts and disagreements into the open and attempts to resolve them collaboratively; builds consensus
  • Manages training new/current employees with respect to documentation, use of equipment, laboratory techniques and department procedures. May routinely monitor or supervise the work of one or more employees. Provides input on performance evaluations to area manager.
  • Work on special projects as they arise
  • Support inspection readiness, participate in regulatory agency inspections and provide audit support, as required.
  • Lead continuous improvement activities for the validation program and revise, create and approve validation documents and procedures
  • Develop technical assessments using engineering principals and standards to support leveraging existing validation studies for changes that do not represent a new worst case.
Knowledge, Skills & Qualifications
  • Has an advanced understanding of validation and regulatory requirements
  • Can assess what work supports the validation strategy and make insightful recommendations regarding priorities
  • Expert inequipment, utilities and facilities domains of validation. Familiar in other areas of domain expertise within the team.
  • Experience using project management tools is a plus.
Education and Experience
  • Bachelor's degree from an accredited college or university
  • 7+ years of validation, science/technical or engineering background required, pharmaceutical validation or engineering experience preferred.
Minimum Qualifications
  • Must be at least 18 years of age
Travel Requirements
  • Typically requires travel less than 5% of the time
Physical Requirements and Work Environment
  • This is largely a sedentary role.
  • This job operates in a professional office environment and routinely uses standard office equipment.
  • Work may be performed in a clean room environment
  • Must be able to occasionally move and lift objects of up to 25 lbs
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What ICU Medical employees say

Pay

Benefits

Hours and flexibility

Workplace

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About ICU Medical

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

San Clemente, CA, US

Year founded

1984

Social media

Twitter

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