ZipRecruiter

Log In

1

From Home Computer System Validation Jobs in Illinois

Next Step Systems

FPGA Engineer - Work From Home

Chicago, IL · On-site +1

$133K - $172K/yr

... and validating and analyzing designs for errors and efficiency - Research, design and develop ... computer science or related technical field. - 9+ years of experience in FPGA design, including ...

Globe Life Inc.

Work From Home Sales

Chicago, IL · Remote

With strong leadership, proven systems, and nationwide growth, we offer careers -- not just jobs. The Opportunity Were hiring driven, coachable individuals ready to grow in a dynamic remote ...

The Semler Agency

Work From Home Sales

Bloomington, IL · On-site +1

This role is designed for individuals looking to learn a new skill and work from home with support ... sales system and engage with our lead system, and the Insurance needs of the customers in the ...

Alliant Credit Union

Lead Model Validation

Chicago, IL · Hybrid

$95K - $163K/yr

... Computer Science or related * Minimum - 5 Years of Build, test, implement, or validate models ... Work from home up to 3 days a week * Paid parental leave * Employee discount programs * Time off ...

McQuade Organization

$15 - $20.50/hr

Maintain accurate records using the company's CRM system. * Follow all company guidelines ... Comfortable using Zoom, email, and basic computer applications.

previous page

Showing results 41-60

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.

What are the most commonly searched types of Computer System Validation jobs in Illinois?

The most popular types of Computer System Validation jobs in Illinois are:

What are popular job titles related to From Home Computer System Validation jobs in Illinois?

For From Home Computer System Validation jobs in Illinois, the most frequently searched job titles are:

What job categories do people searching From Home Computer System Validation jobs in Illinois look for?

The top searched job categories for From Home Computer System Validation jobs in Illinois are:

What cities in Illinois are hiring for From Home Computer System Validation jobs?

Cities in Illinois with the most From Home Computer System Validation job openings:

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.

Business Development Manager- Commissioning, Qualification, Validation (CQV) - Remote from home

Wood Plc

Chicago, IL • On-site, Remote

Full-time

Re-posted 28 days ago

Job description

Overview / Responsibilities

Wood PLC, on a global scale, serves the Pharma-Bio, Oil & Gas, Federal, Infrastructure, Manufacturing, Mining, and Power Industries. Our Philadelphia office has become the center of excellence for our global Life Sciences network. It provides process engineering, process design, and commissioning - qualification - validation (CQV) services to pharmaceutical/biotechnology clients worldwide. For projects of every scale, we provide services that support a facility's entire life cycle to bring life-saving therapeutics from concept through fruition. Learning from our team of industry-leading experts in facility design, regulatory standards, and project management will pay dividends toward your future career.

Our CQV group at Wood is seeking a regional Director of CQV, open to various locations in the United States. The position will be responsible for the regional development, maintenance, and growth of the CQV business.

Primary responsibilities include CQV business development, building a local CQV group (recruiting, interviewing, hiring, team performance), identifying commissioning, qualification and/or validation opportunities, proposal development, project execution, and full responsibility for the profit and loss regional CQV business. This is a seller-doer position. As a candidate you must have the ability to identify opportunities, develop the team, and assist in project execution.

Previous experience as an Engineering/CQV service provider preferred.  Must be thoroughly knowledgeable in pharmaceutical industry cGMPs, commissioning, qualification, validation, and CQV project management.  Must have proven capability in leading project teams, scheduling, coordinating the efforts of a multidisciplinary team and identifying and building client relationships.

Ability to effectively interface directly with clients in representing Wood is essential.

****This position offers a competitive salary, opportunty for growth, and a signing bonus.

Skills / Qualifications

Essential Job Functions/Skills:

  • Effectively lead project teams managing scope, budget, and schedule to ensure project success is required
  • Fostering Wood's relationships with clients, business development
  • Ability to travel to client sites
  • Business development including identifying potential growth areas and development of CQV proposals
  • Hiring of CQV personnel
  • Extensive experience in commissioning/qualification/validation and a thorough understanding of cGMPs
  • Knowledge of the local pharma market
  • Ability to lead and or assist in project execution

Education and Experience Requirements:

  • BS Engineering (Chemical Engineering preferred); Other life sciences may be acceptable; Educational requirements may be relaxed for suitable experience
  • Minimum of 12 years of experience in engineering, commissioning, qualification, and validation primarily in the field of pharmaceuticals
Company Overview

Wood is a global leader in engineering and consultancy across energy and the built environment, helping to unlock solutions to some of the world's most critical challenges. We provide consulting, projects and operations solutions in more than 60 countries, employing around 40,000 people. www.woodplc.com

Diversity Statement

We are an equal opportunity employer that recognises the value of a diverse workforce. All suitably qualified applicants will receive consideration for employment on the basis of objective criteria and without regard to the following (which is a non-exhaustive list): race, colour, age, religion, gender, national origin, disability, sexual orientation, gender identity, protected veteran status, or other characteristics in accordance with the relevant governing laws.

Employment Type: OTHER

Apply