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From Home Computer System Validation Jobs in California

Apple

SerDes System Validation Engineer

Cupertino, CA · On-site

... hear from you...If you thrive on understanding the bigger picture while diving deep into the ... Ownership of SerDes system bring-up, validation and debug. This will involve a SerDes bring up in ...

Apple

SerDes System Validation Engineer

Cupertino, CA · On-site

... hear from you...If you thrive on understanding the bigger picture while diving deep into the ... Ownership of SerDes system bring-up, validation and debug. This will involve a SerDes bring up in ...

Apple

SerDes System Validation Engineer

Cupertino, CA

$126K - $220K/yr

We are looking for a SerDes System Validation Engineer to lead system validation of mixed-signal ... to hear from you. If you thrive on understanding the bigger picture while diving deep into the ...

Apple

SerDes System Validation Engineer

Cupertino, CA · On-site

$181K - $318K/yr

We are looking for a SerDes System Validation Engineer to lead system validation of mixed-signal ... to hear from you. If you thrive on understanding the bigger picture while diving deep into the ...

PSC Biotech

LabWare Specialist

Thousand Oaks, CA

$85K - $115K/yr

Support Computer System Validation (CSV) activities for LabWare implementations and enhancements. * Author and/or contribute to validation deliverables. * Ensure full requirements-to-configuration ...

New

PSC Biotech

LabWare Specialist

Ventura, CA · On-site

Support Computer System Validation (CSV) activities for LabWare implementations and enhancements. * Author and/or contribute to validation deliverables. * Ensure full requirements-to-configuration ...

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All JobsFrom Home Computer System Validation JobsFrom Home Computer System Validation Jobs in California

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
Senior Computer System Validation Consultant

Senior Computer System Validation Consultant

CYNET SYSTEMS

San Diego, CA • On-site

$23 - $28/hr

Contractor

Posted 29 days ago

Job description

Job Overview:
 
Pay Range: $23.98hr - $28.98hr
  • The role involves leading computer system validation activities across the system lifecycle, ensuring regulatory compliance, data integrity, and quality governance in a biopharmaceutical environment, including validation planning, risk management, and audit readiness.

Requirement/Must Have:

  • Bachelor’s degree in Life Sciences or related discipline within the pharmaceutical/biotech industry.
  • Strong experience in CSV (Computer System Validation) and Quality Compliance.
  • Deep understanding of 21 CFR Part 11, GxP (211/820), GAMP 5, and EU Annex 11.
  • Strong knowledge of data integrity and validated systems in regulated environments.
  • Experience with quality management systems including Change Control, Deviations, CAPA, Document Control, Training, EDMS, and LMS.
  • Strong technical understanding of IT systems, networked applications, and infrastructure in regulated environments.
  • Proficiency in MS Excel, PowerPoint, and Word.
  • Strong communication, collaboration, and stakeholder management skills.

Experience:

  • Experience working in life sciences, biotech, or pharmaceutical environments.
  • Experience in validation lifecycle management and compliance oversight.
  • Experience supporting regulated GMP systems and audits.

Responsibilities:

  • Author, review, and approve validation deliverables including validation plans, risk assessments, URS, configuration specifications, test scripts (IQ/OQ/PQ), and validation summary reports.
  • Perform requalification and periodic reviews of existing computer systems.
  • Oversee system development lifecycle processes ensuring compliance across build, test, deploy, and maintenance phases.
  • Act as quality lead for project teams and guide validation and compliance activities.
  • Review and approve system lifecycle documentation to ensure SOP and regulatory compliance.
  • Support and lead internal and external audits and regulatory inspections.
  • Conduct risk assessments and escalate compliance or security issues as required.
  • Prepare compliance and validation status reports for management.
  • Perform gap assessments for legacy systems and integration readiness.
  • Advise teams on implementing security and compliance controls to ensure data integrity.
  • Promote teamwork and align daily activities with organizational quality goals.

Should Have:

  • Strong understanding of laboratory, manufacturing, and quality systems in GMP environments.
  • Experience with cell and gene therapy or pharmaceutical data systems preferred.
  • Strong knowledge of advanced quality systems and validation processes.

Skills:

  • Computer System Validation (CSV).
  • Regulatory compliance (21 CFR Part 11, GxP, GAMP 5, EU Annex 11).
  • Risk management and audit support.
  • Quality systems (CAPA, Change Control, Deviations, Document Control).
  • System lifecycle and validation documentation.
  • MS Office Suite (Excel, Word, PowerPoint).
  • Data integrity and regulated system compliance.

Qualification And Education:

  • Bachelor’s degree in Life Sciences or related field required.

Founded in 2010 and headquartered in the Washington, DC metro area, Cynet Systems Inc. is a leading staffing and recruiting powerhouse. Proudly recognized as a nationally and locally certified diversity firm, Cynet delivers agile, scalable talent solutions across industries. With an active footprint in all 50 U.S. states and Canada, we support thousands of consultants through our expansive, high-performing recruitment engine operating across North America and Asia—ensuring speed, quality, and consistency in every hire.
Cynet Systems logo

About Cynet Systems

Sourced by ZipRecruiter

Cynet Systems Inc is a staffing and recruiting corporation nestled in Ashburn, VA, USA. Established in 2010, the company operates within the Information Technology and Services sector, specializing in providing effective workforce solutions to different business needs, including IT consulting, direct hire, and contract staffing services. Through the years, Cynet Systems has built an impressive portfolio, going beyond borders and expanding its operations internationally in Canada and India. Rooted in its core values of teamwork, leadership, and commitment, Cynet Systems helps businesses unlock their full potential by providing versatile and competent professionals that perfectly align with their needs. Fueled by their unwavering mission to deliver top-tier talent to businesses worldwide, Cynet Systems garnered various recognitions including SIA's fastest-growing staffing firms and Best Place to Work in Virginia for 2019.

Industry

It services

Company size

501 - 1,000 Employees

Headquarters location

Sterling, VA, US

Year founded

2010

Social media

Twitter

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