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Validation Technologist Jobs (NOW HIRING)

Tata Technologies

Validation Engineer

Auburn Hills, MI · On-site

Validation Engineer Auburn Hills, MI Southfield, MI Onsite Job Introduction The Validation Engineer ... These components span a wide range of technologies, including analog, digital, optical, color ...

Trident Consulting

Validation Engineer

Irvine, CA · On-site

$48/hr

Trident Consulting is seeking a " Validation Engineer " for one of our clients in " San Clemente, CA (Onsite)" A global leader in business and technology services. Please find additional details ...

Limitlessli

Validation Analyst

Charlotte, NC · On-site

Technology & Systems Validation * Support validation efforts related to software applications, system enhancements, integrations, upgrades, and configuration changes. * Create and maintain testing ...

CASM Limitlessli

Validation Analyst

Charlotte, NC · On-site

Technology & Systems Validation * Support validation efforts related to software applications, system enhancements, integrations, upgrades, and configuration changes. * Create and maintain testing ...

Limitlessli

Validation Analyst

Charlotte, NC · On-site

Technology & Systems Validation * Support validation efforts related to software applications, system enhancements, integrations, upgrades, and configuration changes. * Create and maintain testing ...

Trident Consulting

Validation Engineer

Irvine, CA · On-site

$55/hr

Hiring: QA / Validation Engineer Location: San Clemente, CA - Onsite Type: 6-Month Contract Rate ... Bachelor's degree in Engineering, Information Technology, Computer Science, or a related field.

Solidigm

Validation Architect

Rancho Cordova, CA · On-site

Solidigm will continue to lead the world in innovating new Memory technologies with aspirations to ... The ideal candidate will drive end-to-end validation across firmware, hardware, platform ...

Agilent

Validation Engineer

Frederick, CO · On-site

Execute validation studies in support of engineering, manufacturing, process development, facilities, IT, quality control, and quality assurance. * Manage or support the validation program. Suggests ...

OSI Engineering, Inc.

Validation Engineer

Cupertino, CA · On-site

$65 - $85/hr

You will be responsible for validating wireless performance across product portfolio. Working hands ... Contribute to evolving wireless characterization methodologies as new cellular technologies emerge.

Solidigm

Validation Architect

Rancho Cordova, CA · On-site

Solidigm will continue to lead the world in innovating new Memory technologies with aspirations to ... The ideal candidate will drive end-to-end validation across firmware, hardware, platform ...

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Validation Technologist information

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How much do validation technologist jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for validation technologist in the United States is $26.09, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $30.53 per hour, depending on experience, location, and employer.

What cities are hiring for Validation Technologist jobs?

Cities with the most Validation Technologist job openings:

What states have the most Validation Technologist jobs?

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Infographic showing various Validation Technologist job openings in the United States as of August 2026, with employment types broken down into 91% Full Time, 4% Part Time, and 5% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $54,267 per year, or $26.1 per hour.

Validation Specialist

Marion, NC • On-site

Accord Technologies Inc.
IT Services • 51 - 200 employees
Learn more about Accord Technologies Inc.external

Contractor

Re-posted 20 days ago

Job description

Validation Specialist
Marion, NC, USA
12 months
W2 contract
 
 
Must have experience supporting medical device manufacturing under ISO 13485 Writing test protocols within KNEAT Gx Knowledge of CQV (Commissioning Qualification and Validation) process
 
 
Required Qualifications: 
• The Validation Specialist (Contract) will support pharmaceutical and medical device operations by executing and maintaining compliant validation activities using Kneat Gx as the electronic validation lifecycle management system
This role is focused on hands on execution of validation deliverables to support equipment, process, utility, and computerized system readiness in accordance with FDA, ISO, and cGMP requirements
• The specialist will work closely with Engineering, Quality, Automation, IT, and Operations to ensure systems and equipment are validated, audit ready, and capable of supporting safe, compliant production
• Validation Execution (Primary Role)
• Execute IQ, OQ, PQ, requalification, and validation maintenance activities for pharma and medical device manufacturing systems.
• Manufacturing and packaging equipment
• Utilities (compressed air, clean utilities, environmental controls)
• Computerized systems (automation, data acquisition, MES, LIMS, vision systems)
• Apply risk-based validation methodologies aligned with GAMP 5 and industry best practices.
Preferred Qualifications:
• Experience supporting medical device manufacturing under ISO 13485.
• Experience with automation and controls (PLC/SCADA), vision systems, or MES.
• Experience supporting high speed packaging or assembly lines.
• Exposure to validation remediation or regulatory commitment work
Required Technical Skills:
• KNEAT Gx Lifecycle Management
• Author, execute, review, and route validation documents within KNEAT Gx.
• Maintain end to end traceability between:
• User Requirements (URS)
• Risk Assessments
• Test cases and protocols
• Deviations and final reports
• Ensure proper use of KNEAT Gx workflows, execution controls, and electronic approvals.
• Maintain compliance with 21 CFR Part 11 and data integrity expectations.
• Deviation, Change Control & CAPA Support
• Document and investigate validation deviations within KNEAT Gx
• Support change control impact assessments affecting validated systems
• Participate in root cause analysis and CAPA implementation when required
Regulatory & Quality Compliance
• Ensure validation deliverables comply with:
• oFDA cGMP regulations (21 CFR Parts 210/211, Part 11)
• ISO 13485 (Medical Devices)
• Internal Quality Management System (QMS) requirements
• Support regulatory inspections and customer audits by providing validation documentation and responses.
• Maintain validation documentation in a state of continuous inspection readiness
Responsibilities:
• Collaborate with Engineering, Quality, IT, Automation, Manufacturing, and external vendors.
• Provide on floor support during commissioning, troubleshooting, and validation execution.
• Support site initiatives such as new equipment introduction, line upgrades, remediation efforts, and capacity expansions.
• Detail oriented with a strong compliance mindset
• Ability to work independently under contract deliverables
• Strong problem solving and root cause analysis skills
• Effective communication with cross functional teams
• Comfortable working in production and controlled environments
• On site support in a controlled GMP manufacturing environment
• May require off shift or weekend support during execution windows
• PPE and gowning requirements may apply depending on area
Additional Details:
• Industry: Pharmaceutical & Medical Devices
• Contract Type: Contract (On site / Hybrid, as required)
• Duration: Contract basis (length defined by project needs)
• On site support in a controlled GMP manufacturing environment
• May require off shift or weekend support during execution windows
• PPE and gowning requirements may apply depending on area