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Computer Validation Jobs in Missouri (NOW HIRING)

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 ...

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

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Computer Validation information

See Missouri salary details

$9

$50

$80

How much do computer validation jobs pay per hour?

As of Aug 11, 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.

Is computer validation a good field?

Computer validation is a specialized field within quality assurance and regulatory compliance, focusing on ensuring that computerized systems meet industry standards such as 21 CFR Part 11. It often requires knowledge of validation protocols, testing, and documentation, and can offer stable employment with opportunities for certification and skill development. The field is considered important in industries like pharmaceuticals and biotech, where system integrity and data accuracy are critical.

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring 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:
Infographic showing various Computer Validation job openings in Missouri as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 11% Part Time, 2% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $105,978 per year, or $51 per hour.

Validation Engineer II

kindeva

Maryland Heights, MO • On-site

Full-time

Posted 6 days ago


Kindeva rating

6.7

Company rating: 6.7 out of 10

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.

What Kindeva employees say

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