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From Home Computer System Validation Jobs in Illinois

Deloitte

System Test and Validation Lead

Chicago, IL · On-site +1

... from complexity and accelerate their path to value creation. Qualifications Required ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Deloitte

System Test and Validation Lead

Chicago, IL · On-site +1

... from complexity and accelerate their path to value creation. Qualifications Required ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Deloitte

System Test and Validation Lead

Chicago, IL · On-site +1

... from complexity and accelerate their path to value creation. Qualifications Required ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

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All JobsComputer System Validation JobsFrom Home Computer System Validation JobsFrom Home Computer System Validation Jobs in Illinois

From Home Computer System Validation information

What is the difference between From Home Computer System Validation vs From Home Quality Assurance Specialist?

AspectFrom Home Computer System ValidationFrom Home Quality Assurance Specialist
CertificationsGxP validation, 21 CFR Part 11ISO 9001, QA certifications
Work EnvironmentPrimarily remote, focused on system testing and validationRemote or onsite, focused on process audits and compliance
Industry UsagePharmaceutical, biotech, healthcareManufacturing, software, healthcare
Job FocusEnsuring computer systems meet regulatory standardsEnsuring overall quality processes and compliance

From Home Computer System Validation primarily involves verifying that computer systems meet regulatory standards, especially in healthcare and biotech industries. In contrast, From Home Quality Assurance Specialist focuses on broader quality processes and compliance across various industries. Both roles may be remote and require similar certifications, but their core responsibilities differ in scope and focus.

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From Home Computer System Validation jobs near you
Infographic showing various From Home Computer System Validation job openings in Illinois as of June 2026, with employment types broken down into 53% Full Time, 44% Part Time, 2% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Computer System Validation (CSV) Engineer

Clappr LLC

Chicago, IL • On-site

$60 - $65/hr

Other

Posted 2 days ago

New

Job description

We're looking for an experienced CSV Engineer to support validation activities across a wide portfolio of regulated systems — from laboratory instrumentation to manufacturing equipment to enterprise platforms. This role acts as the connective tissue between Quality, IT, Lab, and Manufacturing, keeping systems validated and maintained in compliance with 21 CFR Part 11, GxP, and EMA requirements. This is an onsite role reporting to the Sr. Director of IT, and candidates must be authorized to work in the U.S. without current or future sponsorship.


Contract to Hire: $60-$65/hour


What you'll do


  • Plan, author, and execute validation deliverables — including Validation Plans, URS, FS, DS, IQ/OQ/PQ protocols, Traceability Matrices, and Validation Summary Reports — across assigned systems


  • Support CSV activities spanning lab instruments (HPLC, GC, spectrophotometers, balances, and similar), engineering and manufacturing equipment, and enterprise systems such as Caliber LIMS, SAP, and BMRAM


  • Partner with system owners, QA, and IT to keep systems in a validated state through change control and periodic review


  • Execute risk assessments and data integrity assessments aligned with ALCOA+ principles


  • Support audits, inspections, CAPA investigations, and deviations involving computerized systems


  • Collaborate with senior validation leads and subject matter experts to drive consistent validation practices across sites

    • What you'll bring


    • Bachelor's degree in Life Sciences, Engineering, or IT — or equivalent laboratory experience in a life sciences environment


    • Minimum 5 years of CSV experience in a GxP-regulated environment


    • Working knowledge of 21 CFR Part 11, EU Annex 11, and EMA guidance


    • Hands-on experience authoring and executing IQ/OQ/PQ protocols

    • Validation experience with at least two of: laboratory instruments, engineering/manufacturing equipment, LIMS, SAP, or CMMS/calibration platforms (e.g., BMRAM)


    Nice to have


    • Familiarity with GAMP 5 principles and risk-based validation approaches


    • Exposure to Caliber LIMS


    • Exposure to SAP (QM, MM, PP) in a GxP context


    • Experience with BMRAM or an equivalent CMMS/calibration system


    • Prior experience serving as a liaison across IT, Quality, Lab, and Manufacturing teams

    • Benefits & perks

    This is an onsite position in a fast-paced, deadline-driven setting. It may require extended hours or occasional weekend work, and moderate domestic travel. Physical requirements are light 


    Apply