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Senior Validation Engineer Consultant

Katalyst Healthcares and Lifesciences

Massachusetts • Today

Full-time

Commissioning and Qualification (C&Q)/Senior Validation Engineer

Algo Soft Solutions LLC

Harvard, Massachusetts • 5d ago

Easy Apply

Contract

Depends on Experience

Senior CQV Engineer/Senior Validation Engineer Consultant

Katalyst Healthcares and Lifesciences

Massachusetts • Today

Full-time

Senior Engineer Test Method Validation

Innova Solutions, Inc

North Andover, Massachusetts • 7d ago

Easy Apply

Contract

$95 - $107

Hardware & Silicon Validation Senior Staff Engineer

Marvell Semiconductor Inc.

Westborough, Massachusetts • Today

Full-time

USD 143,400.00 - 212,230.00 per year

Sr Engineer - Test Method Validation

VOLT

Andover, Massachusetts • Today

Full-time

USD 100.00 per hour

Senior Engineer, Process Validation

Danaher Corporation

Remote • Today

Full-time

USD 100,000.00 - 130,000.00 per year

Senior Device Validation Engineer

Flock Safety

Remote or Atlanta, Georgia • Today

Full-time

USD 150,000.00 - 190,000.00 per year

Senior Workday Absence SME / Consultant

Kforce Technology Staffing

Remote or Fort Lauderdale, Florida • Today

Contract

$70 - $75 hourly

Senior Consultant II - AI/ML Engineer (.NET Focus)

Allstate Insurance Company

Remote • Today

Full-time

USD 140,000.00 - 150,000.00 per year

Senior Engineering Consultant

Bureau Veritas

Remote • Today

Full-time

USD 95,000.00 per year

Senior Verification Engineer

Analog Devices, Inc.

Wilmington, Massachusetts • Today

Full-time

USD 110,385.00 - 151,808.00 per year

Senior Principal Engineer, Design Verification

Marvell Semiconductor Inc.

Westborough, Massachusetts • Today

Full-time

USD 204,900.00 - 303,250.00 per year

Senior Engineer, Design Verification Engineering

Analog Devices, Inc.

Wilmington, Massachusetts • Today

Full-time

USD 134,597.00 - 165,615.00 per year

API Developer/Data Engineer Managing Consultant-Fraud/AI

Navigant Consulting

Remote or McLean, Virginia • Today

Full-time

USD 130,000.00 - 216,000.00 per year

Senior Azure & Databricks Consultant

Codeforce 360

Remote • Today

Easy Apply

Contract, Third Party

$60 - $65

Sr. Temporal Skill Consultant

BirdsVue LLC

Remote • 14d ago

Easy Apply

Contract

Depends on Experience

Senior Veeva CTMS Consultant (Greenfield Implementation)

Econosoft

Remote • 10d ago

Easy Apply

Contract

Depends on Experience

Senior Oracle Consultant

Robert Half

Remote or Troy, Michigan • Today

Easy Apply

Contract

USD 66.50 - 77.00 per hour

Sr. Conversational AI Consultant

Verint Systems Inc

Remote • Today

Full-time

Senior Microsoft Dynamics 365 Finance & Operations (F&O) Supply Chain Management (SCM) Consultant

HCM Staffing and Consulting

Remote • 7d ago

Easy Apply

Contract

$53 - $58

Senior Workday Total Rewards Consultant - Remote

NTT DATA Americas, Inc

Remote • 20d ago

Easy Apply

Contract, Third Party

$93.33

Adobe Customer Journey Analytics Senior Consultant

Hexaware Technologies, Inc

Remote • 7d ago

Easy Apply

Full-time

$140,000 - $180,000

Senior Consultant - AI

3CLoud

Remote • Today

Full-time

USD 109,800.00 - 164,700.00 per year

Sr. Optical Engineer

Novanta Inc

Bedford, Massachusetts • Today

Full-time

USD 130,000.00 - 175,000.00 per year

Senior UKG / Workday Integration Program Manager (Healthcare)

TalentFish LLC

Remote • Today

Easy Apply

Contract

$75 - $100

Senior Machine Learning Engineer ml/python/Wilmington ma

Motion Recruitment Partners, LLC

Wilmington, Massachusetts • Today

Easy Apply

Full-time

$140000 - $165000

SAP Security/GRC Consultant

Spadtek Solutions LLC

Remote • 4d ago

Easy Apply

Third Party, Contract

Depends on Experience

Braze Consultant - Remote

V-Soft Consulting Group, Inc

Remote • 4d ago

Easy Apply

Contract

Depends on Experience

Empower Configuration Consultant

NTT DATA Americas, Inc

Remote • 26d ago

Easy Apply

Contract, Third Party

$71

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 CQV Engineer / 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: 10a8ea931c68a7716dea6a1abe39fa70
Posted 30+ days ago

Fitment

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Harvard, Massachusetts

•

5d ago

We are seeking a Commissioning and Qualification Engineer to support the installation, startup, commissioning and qualification of new single-use bioprocess equipment. The engineer will work closely with Process Engineering, Automation, CSV, Quality, equipment vendors and Operations. This position requires strong equipment and process knowledge, with the ability to translate process requirements into meaningful commissioning and qualification testing. Senior Validation Engineer Responsibilities:

Easy Apply

Contract

Depends on Experience

Validation Engineer

Chelsea, Massachusetts

•

Today

Validation Engineer Position Summary: Work Schedule: Monday - Friday, 8:00am to 5:00pm100% on-site The Chelsea facility is Catalent's global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest Good Manufacturi

Full-time

USD 89,000.00 - 110,000.00 per year

CSV Engineer

Woburn, Massachusetts

•

Today

Job Summary: We are seeking a Computer System Validation (CSV) Engineer with experience in Computer System Validation (CSV) within a GMP-regulated pharmaceutical or biotechnology environment. The ideal candidate will have expertise in GAMP 5, 21 CFR Part 11, validation lifecycle documentation, and QC laboratory or manufacturing systems validation, while collaborating with cross-functional teams to ensure regulatory compliance. Roles & Responsibilities: Develop, execute, and maintain Computer S

Full-time

Lead CQV Engineer

Concord, New Hampshire

•

Today

Job Description: Lead second shift CQV execution activities across multiple systems and workstreams Coordinate daily execution priorities to recover schedule slippage and maintain timelines Interface with QA, Engineering, and Operations to resolve issues in real time Oversee execution of IQ/OQ protocols and operational verification activities Responsibilities: Drawing walkdowns Equipment and component verification Materials of Construction (MOC) and weld verification Provide oversight for temper

Full-time

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: 10a8ea931c68a7716dea6a1abe39fa70
Posted 30+ days ago

Fitment

Dice Job Match Score™

👤 Reviewing your profile...

Create job alert

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

Harvard, Massachusetts

•

5d ago

Easy Apply

Contract

Depends on Experience

Validation Engineer

Chelsea, Massachusetts

•

Today

Full-time

USD 89,000.00 - 110,000.00 per year

CSV Engineer

Woburn, Massachusetts

•

Today

Full-time

Lead CQV Engineer

Concord, New Hampshire

•

Today

Full-time

Senior Validation Engineer Consultant

Skills

Summary

Dice Job Match Score™

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Senior Validation Engineer Consultant

Job Details

Skills

Summary

Dice Job Match Score™

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