ZipRecruiter

Log In

1

Lifecycle Specialist Computer Jobs (NOW HIRING)

Stryker Group

Staff CAD/Drafting Specialist

Tempe, AZ · On-site

$77K - $129K/yr

Staff CAD / Drafting Specialist Tempe, AZ At Stryker, we believe great design drives great outcomes ... Mentor peers on CAD, Product Lifecycle Management (PLM), and related systems, resolving technical ...

previous page

Showing results 41-60

All JobsLifecycle Specialist Computer Jobs

Lifecycle Specialist Computer information

See salary details

$7

$28

$50

How much do lifecycle specialist computer jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for lifecycle specialist computer in the United States is $28.63, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $35.34 per hour, depending on experience, location, and employer.

What are popular job titles related to Lifecycle Specialist Computer jobs?

For Lifecycle Specialist Computer jobs, the most frequently searched job titles are:

Infographic showing various Lifecycle Specialist Computer job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $59,550 per year, or $28.6 per hour.

Computer System Validation (CSV) Specialist

Wilson, NC • On-site

Validation & Engineering Group, Inc
See more jobs at Validation & Engineering Group, Incexternal

Full-time

Posted 12 days ago

Key responsibilities

  • Support the validation and lifecycle management of GxP computerized systems.

  • Develop, review, and execute validation documentation including URS, specifications, risk assessments, validation plans, protocols, test scripts, traceability matrices, and validation summary reports.

  • Support system implementation, upgrades, enhancements, periodic reviews, and participate in audit and inspection readiness activities.

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Computer System Validation Specialist

Position Summary

We are seeking a Computer System Validation (CSV) Specialist/Engineer to support validation activities for computerized systems in a regulated manufacturing environment. The ideal candidate will have 3–4 years of hands-on CSV experience and a solid understanding of GxP requirements, system lifecycle documentation, and data integrity principles.

Key Responsibilities

  • Support the validation and lifecycle management of GxP computerized systems.
  • Develop, review, and execute validation documentation, including:
    • User Requirements Specifications (URS)
    • Functional/Design Specifications
    • Risk Assessments
    • Validation Plans
    • IQ/OQ/PQ protocols
    • Test Scripts
    • Traceability Matrices
    • Validation Summary Reports
  • Execute and document system testing and ensure appropriate resolution of discrepancies and deviations.
  • Support system implementation, upgrades, enhancements, and periodic reviews.
  • Perform computerized system risk assessments in accordance with applicable regulatory requirements and company procedures.
  • Ensure compliance with 21 CFR Part 11, GxP, data integrity, and electronic records/electronic signature requirements.
  • Collaborate with IT, Engineering, Quality, Manufacturing, Automation, and system owners throughout the system lifecycle.
  • Support change controls, deviations, CAPAs, and system retirement activities as applicable.
  • Assist with audit and inspection readiness activities related to computerized systems.
  • Maintain accurate and complete validation documentation in accordance with approved procedures.

Qualifications

  • Bachelor’s degree in Engineering, Computer Science, Information Technology, Life Sciences, or a related technical discipline.
  • 3–4 years of experience in Computer System Validation (CSV) within a regulated environment, preferably pharmaceutical, biotechnology, medical device, or life sciences manufacturing.
  • Working knowledge of GAMP 5, 21 CFR Part 11, GxP, and data integrity principles.
  • Experience developing and executing computerized system validation documentation and testing.
  • Strong documentation, analytical, and problem-solving skills.
  • Ability to work cross-functionally with technical and quality teams.
  • Strong written and verbal communication skills.

Preferred Qualifications

  • Experience with Power BI for dashboards, reporting, data visualization, or analytics.
  • Experience validating manufacturing, laboratory, quality, or enterprise systems.
  • Experience supporting system upgrades, implementation projects, or digital transformation initiatives.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.