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From Home Computer System Validation Jobs in Raleigh, NC

CAI

Computer Systems Validation Engineer

Raleigh, NC · On-site

$40 - $47.30/hr

... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test ... System & Industry Expertise Support CSV activities across various platforms including MES, DCS ...

Valspec

Validation Engineer

Raleigh, NC · On-site

Requirements * 3+ years of Computer System Validation (CSV) experience with process control, SCADA ... When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from ...

Valspec

Equipment Validation Engineer

Raleigh, NC · On-site

... a team that also includes computer system validation engineers and specialists. Key ... When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from ...

Anveta

CSV Validation Engineer

Cary, NC · Remote

Participate in internal initiatives around Computer Systems Validation Qualifications * Bachelor or Master's degree in Lifesciences or Computer Sciences * 5+ years' experience with Computer Systems ...

MedPharm

QA Systems Manager - eQMS & CSV

Durham, NC · On-site

Training in Computer System Validation in a Pharmaceutical GMP environment and familiarity with GAMP 5 with minimum 5 years' experience working in the pharmaceutical industry preferred. * Familiar ...

MedPharm

QA Systems Manager - eQMS & CSV

Durham, NC · On-site

Training in Computer System Validation in a Pharmaceutical GMP environment and familiarity with GAMP 5 with minimum 5 years' experience working in the pharmaceutical industry preferred. * Familiar ...

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How much do from home computer system validation jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for from home computer system validation in Raleigh, NC is $52.80, according to ZipRecruiter salary data. Most workers in this role earn between $40.67 and $62.64 per hour, depending on experience, location, and employer.

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
Sr/Principal Computer Systems Validation Specialist

Sr/Principal Computer Systems Validation Specialist

KBI Biopharma, Inc.

Durham, NC • On-site

$133K - $183K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago

Job description

Job Description
This individual will provide thought-leadership, expertise, and management of managed validation services to the IT Validation & Compliance infrastructure in a Contract Development and Manufacturing Organization (CDMO) setting. Individual will be responsible for the validation review and approval of enterprise software validation lifecycle deliverables and the validation technical oversite of change controls, CAPAs, and deviations associated with enterprise software. Working closely with partners in Quality Validation, this individual provides strategic and technical expertise for all global software validation related matters, including assurance that all aspects comply with cGMPs, legal, regulatory requirements, and the KBI internal requirements.
Job Responsibilities:
  • Provide oversight of enterprise software validation from a global perspective.
  • Provide validation direction, guidance, review, and approval for validation lifecycle deliverables of enterprise software projects.
  • Provide oversight and management to validation managed services for associated projects
  • Provide validation review and approval of enterprise software change controls, CAPAs, and deviations.
  • Provide support for data integrity global initiatives.
  • Provide expertise and input for global Policies, SOPs, and Templates for IT Enterprise Software

This position will be based in Durham, NC and will require a regular site presence.
Minimum Requirements:
  • (Principal - BS/MS and 15+ years/ Senior - BS/MS and 8+ years) experience in a cGMP environment in a computer systems validation role with demonstrated career growth and accomplishments.
  • Experience in Data Integrity, computer system validation/IT quality in an FDA regulated manufacturing environment. Demonstrated expert knowledge of 21CFR, Part 11, and/or EU Annex 11 as well as current regulatory guidance on Data Integrity.

Salary Range:
$118,000 - $162,800 (Senior)
$133,000 - $183,700 (Principal)
Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, Sabbatical program, 401K matching with 100% vesting in 60 days and employee recognition programs.
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

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