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Computer assembler Jobs in Fairfield, CA

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Last updated: 22 days ago
Computer System Validation engineer

Computer System Validation engineer

Katalyst HealthCares & Life SciencesVacaville, CA
Full-time
As a Computer System Validation (CSV) Engineer specializing in the pharmaceutical industry, you will ensure that computer-based systems such as Manufacturing Execution Systems (MES), process contro...Show moreLast updated: 22 days ago
L2 Computer Service Technician

L2 Computer Service Technician

The Rockridge GroupVacaville, CA, US
Full-time
L2 Computer Service Technician.We are looking to hire a skilled L2 Service / Repair Technician to assist our clients with computer hardware issues. You will be required to work on-site 8 – 5pm M...Show moreLast updated: 30+ days ago
COMPUTER SCIENCE

COMPUTER SCIENCE

Santa Rosa Junior CollegeSonoma County, CA
Full-time +1
Santa Rosa Junior College is currently accepting applications to establish a pool for part-time associate faculty assignments. Associate assignments are temporary, part-time or on-call.This job post...Show moreLast updated: 30+ days ago
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Computer System Validation engineer

Computer System Validation engineer

Katalyst HealthCares & Life SciencesVacaville, CA
22 days ago
Job type
  • Full-time
Job description

Summary :

As a Computer System Validation (CSV) Engineer specializing in the pharmaceutical industry, you will ensure that computer-based systems such as Manufacturing Execution Systems (MES), process control software, and automation platforms comply with GxP, FDA CFR Part , EU Annex , and other applicable regulations.

Roles & Responsibilities :

  • Develop, execute, and review validation deliverables, including Validation Plans, User Requirements Specifications (URS), IQ / OQ / PQ protocols, and Summary Reports.
  • Collaborate with Quality Assurance, IT, Engineering, and Production teams to ensure system compliance and data integrity.
  • Support internal audits and inspections, ensuring readiness and adherence to regulatory expectations.
  • Provide training to stakeholders on validation requirements and best practices.
  • Maintain validation lifecycle documentation and change control records.

Education & Experience :

  • Experience with CSV in a regulated pharmaceutical or biotech environment.
  • Strong knowledge of GxP, FDA CFR Part , and EU Annex .
  • Proficiency in authoring and executing validation documentation.