Search Jobs | Dice.com

573 results (35 new)

Group by company

Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

Pennsylvania • Today

Full-time

Post-Silicon Systems Software Validation Engineer

Arrow Electronics, Inc.

Remote or California • Today

Full-time

USD 87,400.00 - 165,000.00 per year

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

Integration Validation Engineer- VHA Finance

HigherEchelon

Remote • Today

Full-time

Senior Deep Learning Engineer (Computer vision)

TechVirtue LLC

Remote • 4d ago

Easy Apply

Contract

60 - 65

Sr. System Test Engineer - HiL

Torc Robotics

Remote or Ann Arbor, Michigan • Today

Full-time

USD 139,000.00 - 166,800.00 per year

Data Validation Engineer

GlobalLogic Inc.

Remote • 23d ago

Easy Apply

Full-time

100000 - 110000

Controls Engineer, Distributed Control System (DCS)

NAES

Remote or McKittrick, California • Today

Full-time

USD 140,000.00 - 165,000.00 per year

Engineer Pharma Validation

Medline Industries, LP

Remote • Today

Full-time

USD 73,000.00 - 110,000.00 per year

System Engineer II (Cloud)

Accuity

Remote • Today

Full-time

USD 95,000.00 - 125,000.00 per year

Control System Application Engineer

Creative Information Technology Inc

Remote or Charleston, South Carolina • Today

Full-time

GMS Applications Engineer with Energy Management System Exp

Agile Global Solutions, Inc

Remote • 21d ago

Easy Apply

Contract

Depends on Experience

Staff Software Engineer - Secondary Driving System

General Motors

Remote or Sunnyvale, California • Today

Full-time

USD 218,800.00 - 335,300.00 per year

EDI Business Systems Analyst (834 EDI Required)

System One

Remote • Yesterday

Easy Apply

Contract

$42.25

Active Directory Engineer - Directory Services Consolidation

Randstad Digital

Remote or Newport Beach, California • Today

Full-time

USD60 - USD65

Data Engineer

Select Jarvis.com

Remote • Today

Easy Apply

Contract

$60 - $65

Sr Video Streaming Engineer (Android)

STAND 8

Remote • Today

Easy Apply

Contract

$70 - $80 per hour

Senior AI Security Engineer

GDH

Remote • 14d ago

Easy Apply

Third Party, Contract

Depends on Experience

SAP PP Consultant

RAVIN IT SOLUTIONS, Inc

Remote or Hybrid in Fort Worth, Texas • 3d ago

Easy Apply

Contract

Depends on Experience

Data Product Manager (Remote)

Dahl Consulting

Remote • Today

Easy Apply

Contract

Depends on Experience

Data Engineer

Russell, Tobin & Associates

Remote • 29d ago

Easy Apply

Contract

Depends on Experience

ETL Developer

Futuremindz llc

Remote • 21d ago

Easy Apply

Full-time

70,000 - 90,000

RPA UiPath IXP / Intelligent Document Processing Specialist

RiseIT Solutions

Remote • 3d ago

Easy Apply

Contract

Depends on Experience

Business Application & Systems Administrator

Agilent Technologies

Remote or Carpinteria, California • Today

Full-time

USD 93,760.00 - 175,800.00 per year

Kubernetes Platform Infrastructure Architect

Broadcom Corporation

Remote or New Jersey • Today

Full-time

USD 110,800.00 - 177,300.00 per year

Kubernetes Platform Infrastructure Architect

Broadcom Corporation

Remote or Georgia • Today

Full-time

USD 110,800.00 - 177,300.00 per year

Staff Software Engineer, Capacity Engineering

Pinterest, Inc.

Remote or San Francisco, California • Today

Full-time

USD 177,185.00 - 364,795.00 per year

Sr. Engineering Manager, Programmatic Ad Tech, tvScientific

Pinterest, Inc.

Remote or San Francisco, California • Today

Full-time

USD 208,592.00 - 429,454.00 per year

Business Analyst

CGT Staffing

Remote or Pittsburgh, Pennsylvania • 7d ago

Easy Apply

Contract

Depends on Experience

Business Analyst

CGT Staffing

Remote or Pittsburgh, Pennsylvania • 7d ago

Easy Apply

Contract

Depends on Experience

Job Details

Skills

Sarbanes-Oxley
ISO 9000
ITIL
Inspection
Auditing
URS
Testing
Veeva
LIMS
SAP
Collaboration
Biostatistics
Regulatory Affairs
Manufacturing
Computerized System Validation
GxP
GAMP
Corrective And Preventive Action
Management
SOP
Regulatory Compliance
Documentation
Life Sciences

Summary

Job Summary:

Experienced CSV (Computer System Validation) Consultant with expertise in GxP-compliant environments to support validation, compliance, and audit readiness across life sciences systems.
Strong experience in CSV processes, regulatory frameworks, validation documentation, and exposure to clinical and regulatory domains.

Roles & Responsibilities:

Perform Computer System Validation (CSV) activities aligned with 21 CFR Part 11 / 820, GxP, GAMP 5, SOX, EU Annex 11 / Annex 22, ISO 9001, and ITIL.
Ensure audit and inspection readiness.
Conduct periodic reviews, access roster reviews, and audit trail reviews.
Manage deviations, CAPA processes, SOP, and policy compliance.
Author and review URS / FS documents, validation protocols, validation plans & reports, and final summary reports.
Perform risk-based validation and testing aligned with CSA (Computer Software Assurance).
Support validation lifecycle from planning to execution and closure.
Work with platforms such as Veeva Vault Suite, LabWare LIMS, SAP (GxP modules), and BIOVIA Electronic Lab Notebook.
Collaborate with teams across Biostatistics, Clinical & Discovery, Medical Affairs, Pharmacovigilance, Regulatory Affairs, Manufacturing, Quality, and TechOps.

Education & Experience:

8-10 years of experience in Computer System Validation (CSV).
Strong knowledge of GxP regulations, validation frameworks, GAMP 5, and CSA principles.
Experience with CAPA, deviation management, SOP, and policy compliance.
Strong documentation and validation lifecycle experience.
Good understanding of life sciences domain processes.

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: d49973d14c0d71e511eb2d68d32e706
Posted 30+ days ago

Fitment

Dice Job Match Score™

🔗 Matching skills to job...

Create job alert

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

Similar Jobs

CSV Engineer

New Jersey

•

Today

Job Description: 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

Full-time

Verification & Validation Engineer

No location provided

•

Today

Job Title Verification & Validation Engineer Location US (Primary) Category Engineering Job Type Full-Time Compensation Minimum (USD) $130,000 Compensation Maximum (USD) $150,000 Education Bachelor's Degree Minimum Citizenship Status Required U.S Citizen or Permanent Resident Security Clearance Required None Job Description About Science and Technology Corporation (STC): STC is a science, sensors, and systems company founded in 1979. We continually expand our Earth and Space

Full-time

USD 130,000.00 - 150,000.00 per year

Contract role: Pharma Validation Lead at Raritan, NJ (Onsite Hybrid Model)

Hybrid in New Jersey

•

Today

Validation Lead Raritan, NJ (Onsite Hybrid Model) Long Term Contract Job Details: 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on experience in retro-validation activities and 21 CFR remediation projects with knowledge of CSA, GAMP 5, 21 CFR Part 11, Annex 11, and audit/inspection readiness. Experience in the Pharmaceutical, biotechnology, or medical device industry Experience in FDA and/or Global regulated environment with good understandin

Easy Apply

Third Party, Contract

Engineer Pharma Validation

Remote

•

Today

Job Summary Responsible for the validation of facility utilities, equipment processes and cleaning for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements. Assist in authoring and executing protocols to demonstrate that manufacturing and cleaning processes are executed with consistent quality and results within a controlled environment. Responsible for managing and or performing reval

Full-time

USD 73,000.00 - 110,000.00 per year

Job Details

Skills

Sarbanes-Oxley
ISO 9000
ITIL
Inspection
Auditing
URS
Testing
Veeva
LIMS
SAP
Collaboration
Biostatistics
Regulatory Affairs
Manufacturing
Computerized System Validation
GxP
GAMP
Corrective And Preventive Action
Management
SOP
Regulatory Compliance
Documentation
Life Sciences

Summary

Job Summary:

Experienced CSV (Computer System Validation) Consultant with expertise in GxP-compliant environments to support validation, compliance, and audit readiness across life sciences systems.
Strong experience in CSV processes, regulatory frameworks, validation documentation, and exposure to clinical and regulatory domains.

Roles & Responsibilities:

Perform Computer System Validation (CSV) activities aligned with 21 CFR Part 11 / 820, GxP, GAMP 5, SOX, EU Annex 11 / Annex 22, ISO 9001, and ITIL.
Ensure audit and inspection readiness.
Conduct periodic reviews, access roster reviews, and audit trail reviews.
Manage deviations, CAPA processes, SOP, and policy compliance.
Author and review URS / FS documents, validation protocols, validation plans & reports, and final summary reports.
Perform risk-based validation and testing aligned with CSA (Computer Software Assurance).
Support validation lifecycle from planning to execution and closure.
Work with platforms such as Veeva Vault Suite, LabWare LIMS, SAP (GxP modules), and BIOVIA Electronic Lab Notebook.
Collaborate with teams across Biostatistics, Clinical & Discovery, Medical Affairs, Pharmacovigilance, Regulatory Affairs, Manufacturing, Quality, and TechOps.

Education & Experience:

8-10 years of experience in Computer System Validation (CSV).
Strong knowledge of GxP regulations, validation frameworks, GAMP 5, and CSA principles.
Experience with CAPA, deviation management, SOP, and policy compliance.
Strong documentation and validation lifecycle experience.
Good understanding of life sciences domain processes.

Dice Id: 91116760
Position Id: d49973d14c0d71e511eb2d68d32e706
Posted 30+ days ago

Fitment

Dice Job Match Score™

🔗 Matching skills to job...

Create job alert

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

Similar Jobs

CSV Engineer

New Jersey

•

Today

Full-time

Verification & Validation Engineer

No location provided

•

Today

Full-time

USD 130,000.00 - 150,000.00 per year

Contract role: Pharma Validation Lead at Raritan, NJ (Onsite Hybrid Model)

Hybrid in New Jersey

•

Today

Easy Apply

Third Party, Contract

Engineer Pharma Validation

Remote

•

Today

Full-time

USD 73,000.00 - 110,000.00 per year