... validation, computer systems validation, and inspection/packaging validation activities. The ... Manager. Responsibilities • Provide validation support across multiple sites based on business ...
... validation, computer systems validation, and inspection/packaging validation activities. The ... Manager. Responsibilities • Provide validation support across multiple sites based on business ...
... validation, computer systems validation, and inspection/packaging validation activities. The ... Manager. Responsibilities • Provide validation support across multiple sites based on business ...
... validation, computer systems validation, and inspection/packaging validation activities. The ... Manager. Responsibilities • Provide validation support across multiple sites based on business ...
... validation, computer systems validation, and inspection/packaging validation activities. The ... Manager. Responsibilities • Provide validation support across multiple sites based on business ...
... validation, computer systems validation, and inspection/packaging validation activities. The ... Manager. Responsibilities • Provide validation support across multiple sites based on business ...
... validation, computer systems validation, and inspection/packaging validation activities. The ... Manager. Responsibilities • Provide validation support across multiple sites based on business ...
... validation, computer systems validation, and inspection/packaging validation activities. The ... Manager. Responsibilities • Provide validation support across multiple sites based on business ...
System Test and Validation Lead
Saint Louis, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Saint Louis, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Kansas City, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Kansas City, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Kansas City, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Kansas City, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Saint Louis, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Saint Louis, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Saint Louis, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Saint Louis, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Kansas City, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
System Test and Validation Lead
Kansas City, MO · On-site +1
This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...
... validation, computer systems validation, and inspection/packaging validation activities. The ... Manager. Responsibilities • Provide validation support across multiple sites based on business ...
... validation, computer systems validation, and inspection/packaging validation activities. The ... Manager. Responsibilities • Provide validation support across multiple sites based on business ...
**LIMS Validation Specialist - CSV**
Bridgeton, MO · Hybrid
$40 - $70/hr
LIMS Validation Specialist - CSV We are seeking an experienced Computer System Validation (CSV ... management skills. Responsibilities * Lead the development, execution, and completion of CSV ...
New
Quick apply
**LIMS Validation Specialist - CSV**
Bridgeton, MO · Hybrid
$40 - $70/hr
LIMS Validation Specialist - CSV We are seeking an experienced Computer System Validation (CSV ... management skills. Responsibilities * Lead the development, execution, and completion of CSV ...
New
Maintain strong alignment with internal quality systems, change control, and document management processes. * Champion continuous improvement initiatives to enhance validation efficiency and process ...
Maintain strong alignment with internal quality systems, change control, and document management processes. * Champion continuous improvement initiatives to enhance validation efficiency and process ...
Maintain strong alignment with internal quality systems, change control, and document management processes. * Champion continuous improvement initiatives to enhance validation efficiency and process ...
Maintain strong alignment with internal quality systems, change control, and document management processes. * Champion continuous improvement initiatives to enhance validation efficiency and process ...
Maintain strong alignment with internal quality systems, change control, and document management processes. * Champion continuous improvement initiatives to enhance validation efficiency and process ...
Maintain strong alignment with internal quality systems, change control, and document management processes. * Champion continuous improvement initiatives to enhance validation efficiency and process ...
Maintain strong alignment with internal quality systems, change control, and document management processes. * Champion continuous improvement initiatives to enhance validation efficiency and process ...
Maintain strong alignment with internal quality systems, change control, and document management processes. * Champion continuous improvement initiatives to enhance validation efficiency and process ...
Maintain strong alignment with internal quality systems, change control, and document management processes. * Champion continuous improvement initiatives to enhance validation efficiency and process ...
Maintain strong alignment with internal quality systems, change control, and document management processes. * Champion continuous improvement initiatives to enhance validation efficiency and process ...
... Validation Manger. Role Responsibilities * Execute and support qualification activities for ... systems. * Develop and manage qualification lifecycle documentation and activities including ...
... Validation Manger. Role Responsibilities * Execute and support qualification activities for ... systems. * Develop and manage qualification lifecycle documentation and activities including ...
... Validation Manger. Role Responsibilities * Execute and support qualification activities for ... systems. * Develop and manage qualification lifecycle documentation and activities including ...
... Validation Manger. Role Responsibilities * Execute and support qualification activities for ... systems. * Develop and manage qualification lifecycle documentation and activities including ...
... Validation Manger. Role Responsibilities * Execute and support qualification activities for ... systems. * Develop and manage qualification lifecycle documentation and activities including ...
... Validation Manger. Role Responsibilities * Execute and support qualification activities for ... systems. * Develop and manage qualification lifecycle documentation and activities including ...
Computer System Validation Manager information
See Missouri salary details
$44.6K - $54.2K
1% of jobs
$54.2K - $63.8K
4% of jobs
$71.8K is the 25th percentile. Wages below this are outliers.
$63.8K - $73.5K
24% of jobs
$73.5K - $83.1K
9% of jobs
The median wage is $90K / yr.
$83.1K - $92.7K
17% of jobs
$92.7K - $102.4K
8% of jobs
$102.4K - $112K
5% of jobs
$118.5K is the 75th percentile. Wages above this are outliers.
$112K - $121.6K
11% of jobs
$121.6K - $131.3K
8% of jobs
$131.3K - $140.9K
6% of jobs
$140.9K - $150.5K
8% of jobs
$44.6K
$98.9K
$150.6K
How much do computer system validation manager jobs pay per year?
As of Aug 9, 2026, the average yearly pay for computer system validation manager in Missouri is $98,880.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,900.00 and $123,800.00 per year, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as a computer system validation manager, and why are they important?
To thrive as a Computer System Validation Manager, you need expertise in computer system validation regulations (such as GxP, FDA 21 CFR Part 11), strong project management skills, and a background in life sciences or IT. Familiarity with validation lifecycle documentation tools, quality management systems (QMS), and compliance software is often required, along with relevant certifications like PMP or CSV-related credentials. Exceptional attention to detail, analytical thinking, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring regulatory compliance. These skills and qualifications are vital to ensure validated systems meet regulatory standards, minimize compliance risks, and support organizational quality objectives.
What are some common challenges a computer system validation manager faces during system implementation projects?
A Computer System Validation Manager often encounters challenges such as aligning validation activities with evolving regulatory requirements, managing tight project timelines, and coordinating between multiple stakeholders like IT, Quality Assurance, and business users. Ensuring thorough documentation and traceability, while adapting to technology updates or scope changes, can also be demanding. Proactive communication and strong project management skills are essential to mitigate risks and ensure successful, compliant system implementations.
What does a computer system validation manager do?
A Computer System Validation Manager is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, meet all required compliance standards. They oversee the planning, execution, and documentation of validation activities to ensure systems are reliable, accurate, and secure. Their duties include managing validation projects, writing protocols, coordinating with IT and quality assurance teams, and ensuring adherence to regulations like FDA 21 CFR Part 11. This role is critical for maintaining product quality and regulatory compliance.
What is the difference between Computer System Validation Manager vs Computer System Validation Specialist?
| Aspect | Computer System Validation Manager | Computer System Validation Specialist |
|---|---|---|
| Certifications | GAMP, CQE, CSQE | GAMP, CQE, CSQE |
| Work Environment | Management, oversight, strategic planning | Execution, testing, documentation |
| Industry Usage | Pharmaceutical, biotech, regulated industries | Pharmaceutical, biotech, regulated industries |
| Primary Focus | Leading validation projects, team coordination | Performing validation activities, testing |
The main difference between a Computer System Validation Manager and a Computer System Validation Specialist lies in their roles. The manager oversees validation projects, manages teams, and ensures compliance, while the specialist executes validation tasks and documents testing procedures. Both roles require similar certifications and are vital in regulated industries like pharmaceuticals and biotech.
What are the most commonly searched types of Computer System Validation jobs in Missouri? The most popular types of Computer System Validation jobs in Missouri are:
What are popular job titles related to Computer System Validation Manager jobs in Missouri? For Computer System Validation Manager jobs in Missouri, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Manager jobs in Missouri look for? The top searched job categories for Computer System Validation Manager jobs in Missouri are:
- Medical Device Validation Engineer
- Freelance Work From Home Computer System Validation Csv
- Computer Validation
- Computer System Validation
- Senior Computer System Validation Csv
- Computer System Validation Csv Remote
- Commissioning Qualification Validation Cqv
- Pharma Validation
- Director Computer System Validation Csv
- From Home Computer System Validation
What cities in Missouri are hiring for Computer System Validation Manager jobs? Cities in Missouri with the most Computer System Validation Manager job openings:
Kindeva rating
6.7
Based on 9 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 Floater Validation Engineer II provides validation engineering support across two pharmaceutical aseptic manufacturing facilities and one inspection and packaging site. This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers flexible, cross-site validation coverage while executing protocols, performing testing, and authoring validation documentation under the direction of the Validation Manager.
Responsibilities
• Provide validation support across multiple sites based on business priorities.
• Assist in equipment qualification (IQ/OQ/PQ), cleaning validation, process validation, and CSV.
• Execute and author validation protocols and reports.
• Support aseptic manufacturing and inspection/packaging validation activities.
• Issue validation data, protocols, reports, and technical memos.
• Support site change management programs and maintain validated states.
• Assist with Validation Master Plans and Continuous Process Verification activities.
• Review vendor turnover packages and User Requirement Specifications.
Qualifications
- Bachelor’s degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related discipline
- 5+ years of relevant validation or pharmaceutical manufacturing experience, or equivalent combination of education and experience.
- Knowledge of cGMP and regulatory guidance.
- Experience in aseptic manufacturing and inspection/packaging operations.
- Ability to interpret technical documentation and identify deviations.
• Proficiency with Microsoft Office applications.
- Regular travel between sites required; ability to adapt to multiple GMP environments.
