As a Computer System Validation (CSV) Engineer in the pharmaceutical industry, this role is responsible for ensuring that computer-based systems such as Manufacturing Execution Systems (MES), proce...[show_more][last_updated.last_updated_30]
[promoted]
CMOC Computer Maintenance
InDyneTravis Air Force Base, CA, United States
[job_card.full_time] +1
InDyne is a full-service military, civilian and commercial operations company.Our Mission is to provide tailored cost effective, quality services and solutions.
Our Vision is to exceed customer expe...[show_more][last_updated.last_updated_variable_days]
COMPUTER SCIENCE
Santa Rosa Junior CollegeSonoma County, CA
[job_card.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_more][last_updated.last_updated_30]
Computer Service Technician (L2)
The Rockridge GroupVacaville, CA, US
[job_card.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_more][last_updated.last_updated_30]
Computer System Validation Engineer
Katalyst HealthCares & Life SciencesVacaville, CA
[job_card.30_days_ago]
[job_preview.job_type]
[job_card.full_time]
[job_card.job_description]
Job Summary :
As a Computer System Validation (CSV) Engineer in the pharmaceutical industry, this role is responsible for ensuring 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 regulatory requirements.
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 Computer System Validation (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.