The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
Validation Associate
Kansas City, MO · On-site
$23 - $26/hr
This position serves as a validation representative for laboratory validation activities, including ... Bachelor s Degree in Life Sciences, Physical Science, Computer Science or Engineering field with ...
Validation Associate
Kansas City, MO · On-site
$23 - $26/hr
This position serves as a validation representative for laboratory validation activities, including ... Bachelor s Degree in Life Sciences, Physical Science, Computer Science or Engineering field with ...
Validation Associate
Kansas City, MO · On-site
$23 - $26/hr
This position serves as a validation representative for laboratory validation activities, including ... Bachelor s Degree in Life Sciences, Physical Science, Computer Science or Engineering field with ...
Validation Associate
Kansas City, MO · On-site
$23 - $26/hr
This position serves as a validation representative for laboratory validation activities, including ... Bachelor s Degree in Life Sciences, Physical Science, Computer Science or Engineering field with ...
Validation Engineer II
Saint Louis, MO · On-site
This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...
Validation Engineer II
Saint Louis, MO · On-site
This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...
Validation Engineer II
Saint Louis, MO · On-site
This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...
Validation Engineer II
Saint Louis, MO · On-site
This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...
This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...
This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...
This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...
This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...
... Computer Science, IT, Engineering, Science or equivalent experience Preferred minimum 1-2 years of relevant validation testing in a regulated environment, and team and project experience Software ...
... Computer Science, IT, Engineering, Science or equivalent experience Preferred minimum 1-2 years of relevant validation testing in a regulated environment, and team and project experience Software ...
Validation Engineer II
Saint Louis, MO · On-site
This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...
Validation Engineer II
Saint Louis, MO · On-site
This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...
Equipment & System Validation
Kansas City, MO · On-site
$26/hr
Bachelor's or higher Degree in Life Sciences, Physical Science, Computer Science or Engineering ... For instant consideration for this for Associate, Validation. Position with Adecco KANSAS CITY, MO.
Quick apply
Equipment & System Validation
Kansas City, MO · On-site
$26/hr
Bachelor's or higher Degree in Life Sciences, Physical Science, Computer Science or Engineering ... For instant consideration for this for Associate, Validation. Position with Adecco KANSAS CITY, MO.
Lead Validation Eng
Saint Louis, MO · On-site
The position will also have responsibilities for the review/approval of validation activities for enterprise computer system software and other validation activities as needed to support the ...
Lead Validation Eng
Saint Louis, MO · On-site
The position will also have responsibilities for the review/approval of validation activities for enterprise computer system software and other validation activities as needed to support the ...
The position will also have responsibilities for the review/approval of validation activities for enterprise computer system software and other validation activities as needed to support the ...
The position will also have responsibilities for the review/approval of validation activities for enterprise computer system software and other validation activities as needed to support the ...
Inventory Validation Technician
Saint Louis, MO · On-site
$18.49/hr
Basic computer skills required. Interpersonal Savvy - Relates well to all kinds of people; Builds ... Valid Driver's license required due to variable travel requirements depending on the assigned site ...
Inventory Validation Technician
Saint Louis, MO · On-site
$18.49/hr
Basic computer skills required. Interpersonal Savvy - Relates well to all kinds of people; Builds ... Valid Driver's license required due to variable travel requirements depending on the assigned site ...
Perform Validation Preparation * Create Master Validation Plan as required by the FDA and other ... Computer Crossmatch (if enabled) * Correct Inventory - Demographics * Dispense and Assign * Final ...
Quick apply
Perform Validation Preparation * Create Master Validation Plan as required by the FDA and other ... Computer Crossmatch (if enabled) * Correct Inventory - Demographics * Dispense and Assign * Final ...
Responsibilities : • Execute computer system and equipment validation activities under the guidance of validation leads. • Develop, review, and execute validation protocols (IQ/OQ/PQ), test ...
Responsibilities : • Execute computer system and equipment validation activities under the guidance of validation leads. • Develop, review, and execute validation protocols (IQ/OQ/PQ), test ...
Associate QA Software Validation Engineer
Hazelwood, MO · On-site
$70K - $94.50K/yr
Execute computer system and equipment validation activities under the guidance of validation leads. * Develop, review, and execute validation protocols (IQ/OQ/PQ), test scripts, and reports. * Review ...
Associate QA Software Validation Engineer
Hazelwood, MO · On-site
$70K - $94.50K/yr
Execute computer system and equipment validation activities under the guidance of validation leads. * Develop, review, and execute validation protocols (IQ/OQ/PQ), test scripts, and reports. * Review ...
Computer Validation information
See Missouri salary details
$9.92 - $16.36
2% of jobs
$16.36 - $22.79
9% of jobs
$22.79 - $29.23
1% of jobs
$29.23 - $35.67
4% of jobs
$39.58 is the 25th percentile. Wages below this are outliers.
$35.67 - $42.10
15% of jobs
$42.10 - $48.54
9% of jobs
The median wage is $53.90 / hr.
$48.54 - $54.98
13% of jobs
$60.10 is the 75th percentile. Wages above this are outliers.
$54.98 - $61.41
29% of jobs
$61.41 - $67.85
12% of jobs
$67.85 - $74.29
2% of jobs
$74.29 - $80.72
5% of jobs
$9
$50
$80
How much do computer validation jobs pay per hour?
As of Jun 1, 2026, the average hourly pay for computer validation in Missouri is $50.95, according to ZipRecruiter salary data. Most workers in this role earn between $39.23 and $60.43 per hour, depending on experience, location, and employer.
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 are popular job titles related to Computer Validation jobs in Missouri? For Computer Validation jobs in Missouri, the most frequently searched job titles are:
What job categories do people searching Computer Validation jobs in Missouri look for? The top searched job categories for Computer Validation jobs in Missouri are:
- Commissioning Qualification Validation Cqv
- Validation Engineer Iq Oq Pq
- From Home Computer System Validation
- Freelance Work From Home Computer System Validation Csv
- Medical Device Validation Engineer
- Director Computer System Validation Csv
- Computer System Validation Csv Remote
- Computer System Validation
- Computer System Validation Manager
- Biotech Csv
Other
Posted 16 days ago
Kindeva rating
6.8
Based on 6 frontline employees who took The Breakroom Quiz
Job description
Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated, maintained, and compliant with applicable regulatory requirements including FDA 21 CFR Part 11, EU Annex 11, and GAMP 5 guidelines.
This role supports the full lifecycle of computerized systems including implementation, qualification, maintenance, periodic review, and retirement, ensuring data integrity, system reliability, and inspection readiness across multiple sites or facilities.
Responsibilities
- Validation Lifecycle Execution
- Lead and/or support validation activities for GxP computerized systems including MES, SCADA/PLC, LIMS, EM systems, and serialization/packaging systems
- Author and execute validation documentation: URS, FS/DS, Risk Assessments, IQ/OQ/PQ, Traceability Matrices, Periodic Reviews / Audit Trail Reviews
- Ensure validation deliverables meet internal SOPs and regulatory expectation
- Regulatory Compliance & Data Integrity
- Ensure compliance with 21 CFR Part 11, EU Annex 11, and ALCOA+ principles
- Perform periodic reviews of validated systems
- Support FDA, EMA, and internal audits/inspections
- Assess and remediate data integrity risks
- Change Control & Lifecycle Management
- Support system changes through formal change control processes
- Evaluate impact of updates, patches, and configuration changes
- Ensure appropriate re-validation activities
- Maintain systems in a validated state
- Risk-Based Validation Strategy
- Apply GAMP 5 risk-based validation approach
- Classify systems based on complexity and GxP impact
- Lead risk assessments (FMEA, system risk ranking)
- Cross-Functional Collaboration
- Partner with IT, QA, Manufacturing, MS&T, and Engineering
- Provide CSV guidance during system implementation and facility startup
- Support digital transformation initiatives
- Documentation & Inspection Readiness
- Maintain GMP-compliant validation documentation
- Ensure audit readiness and traceability
- Support responses to audit findings and regulatory observations
- Continuous Improvement
- Improve validation processes and templates
- Support implementation of electronic validation systems (e.g., Kneat, Veeva)
- Drive standardization across sites
Qualifications
- Bachelor’s degree in Engineering, Computer Science, Information Systems, Life Sciences, or related field
- Minimum of 5 years in Computer System Validation in GMP-regulated pharmaceutical or biotech environments
- Experience with manufacturing and laboratory systems validation
- Hands-on experience with Part 11 / Annex 11 compliance
- Strong knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, and ALCOA+
- Familiarity with MES, ERP, LIMS, SCADA/PLC systems
- Understanding of system architecture, interfaces, backup, disaster recovery, and cybersecurity
- Experience in aseptic/sterile injectable manufacturing preferred
- Multi-site validation program experience preferred
- Familiarity with serialization, AVI systems, and cold storage monitoring preferred
- Experience with Kneat, ValGenesis, or Veeva is desirable
- Experience with facility startup and commissioning
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About Kindeva
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