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Senior Validation Engineer

Katalyst Healthcares and Lifesciences

Rock Hill, South Carolina • Today

Full-time

ADAS Calibration & Validation Engineer

Scout Motors

Charlotte, North Carolina • Today

Full-time

USD 140,000.00 - 170,000.00 per year

ADAS Calibration and Validation Engineer

Scout Motors

Charlotte, North Carolina • Today

Full-time

USD 130,000.00 - 160,000.00 per year

Senior Engineer, Process Validation

Danaher Corporation

Remote • Today

Full-time

USD 100,000.00 - 130,000.00 per year

Validation Engineer

Katalyst Healthcares and Lifesciences

Rock Hill, South Carolina • Today

Full-time

Staff Systems Engineer - Release Strategy & Validation

Torc Robotics

Remote or Ann Arbor, Michigan • Today

Full-time

USD 168,800.00 - 202,600.00 per year

Post-Silicon Systems Software Validation Engineer

Arrow Electronics, Inc.

Remote or California • Today

Full-time

USD 87,400.00 - 165,000.00 per year

SKU Qualification Lead Engineer/Hardware Validation Engineer

Galactic Minds Inc.

Remote • 8d ago

Easy Apply

Third Party, Contract

Depends on Experience

Integration Validation Engineer- VHA Finance

HigherEchelon

Remote • Today

Full-time

Sr Generative AI Scientist II - (Model Risk & Validation)

Cotiviti

Remote • Today

Full-time

USD 145,000.00 - 170,000.00 per year

Data Validation Engineer

GlobalLogic Inc.

Remote • 16d ago

Easy Apply

Full-time

100000 - 110000

Engineer Pharma Validation

Medline Industries, LP

Remote • Today

Full-time

USD 73,000.00 - 110,000.00 per year

System Test and Validation Lead

Deloitte

Remote or Atlanta, Georgia • Today

Full-time

USD 95,000.00 - 145,000.00 per year

Data Center Infrastructure Validation - Innovation Lead

EPRI

Remote or Washington, District of Columbia • Today

Full-time

USD 185,000.00 - 200,000.00 per year

AVP, Model Validation

Synchrony Financial

Charlotte, North Carolina • Today

Full-time

Software Engineer L5 - Edge Platform Automation & Validation

Netflix, Inc.

Remote • Today

Full-time

USD 388,000.00 - 619,000.00 per year

Generative AI Scientist - (Model Risk & Validation)

Cotiviti

Remote • Today

Full-time

USD 110,000.00 - 130,000.00 per year

Job Details

Skills

Drawing
P&ID
Regulatory Compliance
SIP
Collaboration
Quality Assurance
Manufacturing
Project Implementation
Lifecycle Management
Document Management
Startups
Continuous Improvement
Biomedical Engineering
Chemical Engineering
GMP
GDP
Documentation
IQ
OQ
Management
Mapping
Chromatography

Summary

Job Description:
Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ protocols, equipment verification, temperature mapping, SIP/CIP validation activities, deviation support, and ensuring compliance with GMP/GDP standards while collaborating with Engineering, QA, and Operations teams.
Roles & Responsibilities:

Execute Installation Qualification (IQ) and Operational Qualification (OQ) protocols for process equipment and utility systems.
Perform drawing walkdowns, including P&ID reviews and system verification activities to ensure equipment installation compliance.
Conduct equipment and component verification activities during commissioning and qualification phases.
Support Management of Change (MOC) activities and perform weld verification as part of validation and compliance processes.
Perform and support temperature mapping studies using data loggers and validation tools such as Ellab.
ssist with Steam-In-Place (SIP) and Clean-In-Place (CIP) execution, cycle development, and validation activities.
Identify, document, and investigate deviations encountered during qualification and validation activities.
Ensure accurate, complete, and compliant documentation in accordance with GMP and GDP requirements.
Collaborate cross-functionally with Engineering, Quality Assurance (QA), Manufacturing, and Operations teams to support project execution and validation deliverables.
Support field verification activities and ensure validation activities meet regulatory and quality standards.
Utilize validation lifecycle management systems such as eVal and support documentation management within validation systems.
Participate in equipment startup, operational readiness, and continuous improvement initiatives for validated systems and processes

Requirements:

Bachelor's degree in STEM, Biomedical Engineering, Chemical Engineering, or a related technical discipline preferred.
3-8 years of CQV (Commissioning, Qualification & Validation) and/or Validation Engineering experience in GMP-regulated industries.
Hands-on experience executing validation activities for process equipment and utility systems.
Strong understanding of GMP/GDP requirements and validation documentation practices.
Experience with IQ/OQ execution, field verification, and equipment qualification activities.
Proficiency with eVal validation management system; experience with ValGenesis is a plus.
Exposure to temperature mapping activities and validation tools such as Ellab preferred.
Experience working with bioprocess equipment including bioreactors, filtration systems, chromatography systems, and ultrafiltration (UF) preferred.
bility to support second-shift operations and weekend work as required.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: cb5665cd2c90667d12f7c7ffd5039250
Posted 30+ days ago

Fitment

Dice Job Match Score™

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Similar Jobs

CQV Engineer

Concord, North Carolina

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Today

Summary : Seeking a CQV Validation Engineer experience in pharmaceutical, biotech, or life sciences. The ideal candidate will have hands-on experience with Commissioning, Qualification & Validation (CQV) for standalone manufacturing equipment in a GMP-regulated environment. Roles & Responsibilities : Perform CQV activities for standalone equipment. Author and execute IQ/OQ/PQ protocols, validation plans, and reports. Support FAT, SAT, commissioning, qualification, and validation activities.

Full-time

Validation Engineer

Rock Hill, South Carolina

•

Today

Responsibilities: Client is seeking validation consultants to support a 9-month minimum onsite project in South Carolina. The consultants will support validation execution and gap assessments tied to equipment qualification, tank qualification, mixing studies, smoke studies, aseptic technique, and instrument/equipment qualification. The project is being driven by audit findings and identified gaps in the site's validation program. The primary focus will be equipment validation, especially around

Full-time

Lead Validation Engineer

New Jersey

•

Today

Job Description: The Lead Validation Engineer leads GMP equipment installation, commissioning, and qualification projects supporting large-molecule biologics manufacturing. This role supports upstream and downstream processes and ensures projects are executed safely, on schedule, and in compliance with regulatory and quality requirements. Responsibilities: Lead end-to-end CQV execution for GMP equipment projects, managing activities from installation through IQ, OQ, and PQ for biologics manufact

Full-time

Senior Engineer, Process Validation

Remote

•

Today

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the spee

Full-time

USD 100,000.00 - 130,000.00 per year

Job Details

Skills

Drawing
P&ID
Regulatory Compliance
SIP
Collaboration
Quality Assurance
Manufacturing
Project Implementation
Lifecycle Management
Document Management
Startups
Continuous Improvement
Biomedical Engineering
Chemical Engineering
GMP
GDP
Documentation
IQ
OQ
Management
Mapping
Chromatography

Summary

Execute Installation Qualification (IQ) and Operational Qualification (OQ) protocols for process equipment and utility systems.
Perform drawing walkdowns, including P&ID reviews and system verification activities to ensure equipment installation compliance.
Conduct equipment and component verification activities during commissioning and qualification phases.
Support Management of Change (MOC) activities and perform weld verification as part of validation and compliance processes.
Perform and support temperature mapping studies using data loggers and validation tools such as Ellab.
ssist with Steam-In-Place (SIP) and Clean-In-Place (CIP) execution, cycle development, and validation activities.
Identify, document, and investigate deviations encountered during qualification and validation activities.
Ensure accurate, complete, and compliant documentation in accordance with GMP and GDP requirements.
Collaborate cross-functionally with Engineering, Quality Assurance (QA), Manufacturing, and Operations teams to support project execution and validation deliverables.
Support field verification activities and ensure validation activities meet regulatory and quality standards.
Utilize validation lifecycle management systems such as eVal and support documentation management within validation systems.
Participate in equipment startup, operational readiness, and continuous improvement initiatives for validated systems and processes

Requirements:

Bachelor's degree in STEM, Biomedical Engineering, Chemical Engineering, or a related technical discipline preferred.
3-8 years of CQV (Commissioning, Qualification & Validation) and/or Validation Engineering experience in GMP-regulated industries.
Hands-on experience executing validation activities for process equipment and utility systems.
Strong understanding of GMP/GDP requirements and validation documentation practices.
Experience with IQ/OQ execution, field verification, and equipment qualification activities.
Proficiency with eVal validation management system; experience with ValGenesis is a plus.
Exposure to temperature mapping activities and validation tools such as Ellab preferred.
Experience working with bioprocess equipment including bioreactors, filtration systems, chromatography systems, and ultrafiltration (UF) preferred.
bility to support second-shift operations and weekend work as required.

Dice Id: 91116760
Position Id: cb5665cd2c90667d12f7c7ffd5039250
Posted 30+ days ago

Fitment

Dice Job Match Score™

🛠️ Calibrating flux capacitors...

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

CQV Engineer

Concord, North Carolina

•

Today

Full-time

Validation Engineer

Rock Hill, South Carolina

•

Today

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Lead Validation Engineer

New Jersey

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Full-time

Senior Engineer, Process Validation

Remote

•

Today

Full-time

USD 100,000.00 - 130,000.00 per year