Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
... validation exceptions/deviations for Computer and IT systems. b. Expertise in MES/Delta-V/LIMS/Lab Equipment and Manufacturing CSV systems. Schedules and executes validations per ASTM, GAMP V ...
... validation exceptions/deviations for Computer and IT systems. b. Expertise in MES/Delta-V/LIMS/Lab Equipment and Manufacturing CSV systems. Schedules and executes validations per ASTM, GAMP V ...
Computer Systems Validation Engineer
$80K - $100K/yr
Join us as a Computer Systems Validation Engineer! Join Abeona Therapeutics Inc. as a Computer Systems Validation Engineer and be part of a mission-driven organization devoted to putting patients ...
Computer Systems Validation Engineer
$80K - $100K/yr
Join us as a Computer Systems Validation Engineer! Join Abeona Therapeutics Inc. as a Computer Systems Validation Engineer and be part of a mission-driven organization devoted to putting patients ...
We are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation ...
Quick apply
We are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation ...
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Computer Systems Validation Engineer
Cleveland, OH · On-site
$80K - $100K/yr
Join us as a Computer Systems Validation Engineer! Join Abeona Therapeutics Inc. as a Computer Systems Validation Engineer and be part of a mission-driven organization devoted to putting patients ...
Quick apply
Computer Systems Validation Engineer
Cleveland, OH · On-site
$80K - $100K/yr
Join us as a Computer Systems Validation Engineer! Join Abeona Therapeutics Inc. as a Computer Systems Validation Engineer and be part of a mission-driven organization devoted to putting patients ...
L.C. is seeking a Computer System Validation Engineer to lead and execute validation activities for GxP electronic systems and applications. The role involves partnering with Business Owners ...
L.C. is seeking a Computer System Validation Engineer to lead and execute validation activities for GxP electronic systems and applications. The role involves partnering with Business Owners ...
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Quick apply
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Required Skills: • Strong Computer Systems Validation (CSV) experience • Familiarity with Manufacturing Execution Systems (MES) • Protocol drafting and execution, good communication • ...
Required Skills: • Strong Computer Systems Validation (CSV) experience • Familiarity with Manufacturing Execution Systems (MES) • Protocol drafting and execution, good communication • ...
Tata Consultancy Services is seeking a Computer System Validation Lead to oversee compliance and validation activities in regulated environments. The role involves leading CSV activities, authoring ...
Tata Consultancy Services is seeking a Computer System Validation Lead to oversee compliance and validation activities in regulated environments. The role involves leading CSV activities, authoring ...
Primarily responsible for ensuring adherence to computer validations, data integrity standards, and procedures for computer related analytical laboratory instruments. Responsibilities include ...
Primarily responsible for ensuring adherence to computer validations, data integrity standards, and procedures for computer related analytical laboratory instruments. Responsibilities include ...
Computer System Validation Engineer
New Brunswick, NJ · On-site
$60/hr
Position- Computer System Validation Engineer Location- New Brunswick, NJ (Onsite) * Rate- $60/hr on C2C/1099 Max JD: * Requirements review * Script Review * Prepare Test/Validation plan
Computer System Validation Engineer
New Brunswick, NJ · On-site
$60/hr
Position- Computer System Validation Engineer Location- New Brunswick, NJ (Onsite) * Rate- $60/hr on C2C/1099 Max JD: * Requirements review * Script Review * Prepare Test/Validation plan
Katalyst CRO is seeking a Computer System Validation (CSV) Engineer for a global pharmaceutical client. This role involves leading and executing validation activities for GxP electronic systems and ...
Katalyst CRO is seeking a Computer System Validation (CSV) Engineer for a global pharmaceutical client. This role involves leading and executing validation activities for GxP electronic systems and ...
Katalyst CRO is seeking a Computer System Validation Engineer for a global pharmaceutical client. This role will lead and execute validation activities for GxP electronic systems and applications ...
Katalyst CRO is seeking a Computer System Validation Engineer for a global pharmaceutical client. This role will lead and execute validation activities for GxP electronic systems and applications ...
Computer systems integrations and validation experience in regulated operations (preferably GMP operations). * Strong experience authoring and executing validation documentation (test scripts ...
Computer systems integrations and validation experience in regulated operations (preferably GMP operations). * Strong experience authoring and executing validation documentation (test scripts ...
Computer System Validation Engineer
Tustin, CA · On-site
$82K - $104K/yr
The Computer System Validation Engineer is responsible for providing technical validation support for manufacturing equipment, laboratory instruments, computer systems, networks, and software that ...
Computer System Validation Engineer
Tustin, CA · On-site
$82K - $104K/yr
The Computer System Validation Engineer is responsible for providing technical validation support for manufacturing equipment, laboratory instruments, computer systems, networks, and software that ...
Computer Systems Validation Engineer Client: Medical Device Manufacturing Company Location: Maple Grove, MN 55311 Duration: 6 Months Contract Focus Area: FDA-regulated Medical Device Software/Systems ...
Computer Systems Validation Engineer Client: Medical Device Manufacturing Company Location: Maple Grove, MN 55311 Duration: 6 Months Contract Focus Area: FDA-regulated Medical Device Software/Systems ...
Substantial experience in in equipment and/or computer validations. Must have Working experience with Controls Automation, Process Control Systems, Distributed Systems, Manufacturing Execution ...
Quick apply
Substantial experience in in equipment and/or computer validations. Must have Working experience with Controls Automation, Process Control Systems, Distributed Systems, Manufacturing Execution ...
Computer Systems Validation Engineer-12345 About This Role: * To ensure the quality of our client's software applications and equipment by validating/qualifying to specifications. * Provide ...
Computer Systems Validation Engineer-12345 About This Role: * To ensure the quality of our client's software applications and equipment by validating/qualifying to specifications. * Provide ...
Computer System Validation Lead
Wilmington, DE · On-site
$100K - $120K/yr
Must Have Technical/Functional Skill • 810 years of experience in Computer System Validation (CSV) in regulated (GxP) environments (Pharma / Biotech / MedTech). • Hands-on experience with ...
Computer System Validation Lead
Wilmington, DE · On-site
$100K - $120K/yr
Must Have Technical/Functional Skill • 810 years of experience in Computer System Validation (CSV) in regulated (GxP) environments (Pharma / Biotech / MedTech). • Hands-on experience with ...
Computer Validation information
See salary details
$10.58 - $17.44
2% of jobs
$17.44 - $24.30
9% of jobs
$24.30 - $31.16
1% of jobs
$31.16 - $38.02
4% of jobs
$42.19 is the 25th percentile. Wages below this are outliers.
$38.02 - $44.89
15% of jobs
$44.89 - $51.75
9% of jobs
The median wage is $57.47 / hr.
$51.75 - $58.61
13% of jobs
$64.07 is the 75th percentile. Wages above this are outliers.
$58.61 - $65.47
29% of jobs
$65.47 - $72.33
12% of jobs
$72.33 - $79.20
2% of jobs
$79.20 - $86.06
5% of jobs
$10
$54
$86
How much do computer validation jobs pay per hour?
Can computer engineers make $500,000?
What is the difference between Computer Validation vs Quality Assurance Specialist?
| Aspect | Computer Validation | Quality Assurance Specialist |
|---|---|---|
| Required Credentials | GxP, 21 CFR Part 11, validation certifications | ISO standards, QA certifications, GxP knowledge |
| Work Environment | Pharmaceutical, biotech, regulated industries | Manufacturing, healthcare, regulated industries |
| Employer & Industry Usage | Regulated industries requiring validated systems | Ensuring quality compliance across processes |
Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.
What is the salary of a CSV engineer?
Is computer system validation a good field?
Is CSV a skill?

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 26 days ago
Job description
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries.
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls, assessment plans, risk assessment reports, compliance plans, user requirements, system and user acceptance testing protocols, traceability matrix, error reports/defect report forms and summary reports. The individual will contribute directly to the completion of projects through the management of assigned contract personnel, development and execution of validation change control documents, and development and review of protocols, reports and data tables generated by peers and contract personnel. Responsibilities include:
- Optimization of CQV support process, including developing including developing standards and KPI reports.
- Compile and analyze validation data and make recommendations for changes and/or improvements
- Maintain all documentation pertaining to computer systems validation
- Data integrity qualification
- Participate in cross-functional project teams including development & deployment teams as well as customer Manufacturing, Engineering, Quality and other groups
- Some travel is required
Skill level & requirements:
- Experience with IQ, OQ, PQ Final reports relating to Computer Systems Validation.
- Experience writing validation master plans.
- Experience with Configuration, design, data and traceability matrices.
- Validation experience with automated systems is preferred
- Thorough knowledge of cGMP regulations related to CSV including 21 CFR Part 11
- Strong knowledge of computerized system development life cycle approach is required
- Strong leadership skills and the ability to work in cross-functional team environments, as well as independently
- Experience coordinating Quality documentation, specifically qualification/Validation documentation
- Demonstrated excellent leadership/Project Manager skills
- Strong technical writing skills
- Excellent written and verbal communication skills
- The ability to work and make decisions independently and have the flexibility to adapt to changing priorities is required
Minimum Requirements:
- Bachelor's degree in a technical discipline (i.e. Engineering, Chemistry, Microbiology, Biology)
- 3 - 5 years Computer Systems Validation background
- 3 - 5 years IT Quality Assurance / Validation experience
- Current driver's license and auto insurance or other means of independent transportation
Quality Agents offers a full suite of benefits for full-time employees including:
- Health, dental and vision insurance
- Life, AD&D and Disability Insurance
- Health savings account for participants in our health plan
- 401k retirement plan
- Paid time off
- Paid holidays
Quality Agents accepts applications on an on-going basis in order to build a talent pool of potential candidates. These applications remain open for consideration, as positions become available, for one (1) year from the date of application.After that time, or if your application information changes, please submit your application again.
About Quality Agents
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
11 - 50 Employees
Headquarters location
Wilmington, NC, US
Year founded
2010