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Computer Validation Jobs in Cincinnati, OH (NOW HIRING)

Investigates and resolves computer software and hardware problems of users. * Serves as a contact ... Must have a valid Driver's License * Experience with Microsoft Active Directory * Experience with ...

Computer skills including knowledge of mailroom equipment: copy machine, package tracking software, postage, etc. * Must have a valid driver's license and car * Vehicle must be insured at all times ...

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Computer Validation information

See Cincinnati, OH salary details

$9

$50

$79

How much do computer validation jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for computer validation in Cincinnati, OH is $50.42, according to ZipRecruiter salary data. Most workers in this role earn between $38.85 and $59.81 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 Cincinnati, OH? For Computer Validation jobs in Cincinnati, OH, the most frequently searched job titles are:
What job categories do people searching Computer Validation jobs in Cincinnati, OH look for? The top searched job categories for Computer Validation jobs in Cincinnati, OH are:
Infographic showing various Computer Validation job openings in Cincinnati, OH as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 3% Contract, and 1% Nights. Highlights an 80% Physical, 1% Hybrid, and 19% Remote job distribution, with an average salary of $104,873 per year, or $50.4 per hour.

Senior Manufacturing Engineer

Meridian Bioscience, Inc.

Cincinnati, OH • On-site

$87K - $119K/yr

Other

Posted 2 days ago

New


Job description

About Meridian
Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy and simplicity that are redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals that help drive our vision. Our innovative culture will allow interested candidates to discover and create, through collaboration, cutting edge solutions to tough problems.
Job Summary
The Senior Process Engineer is responsible for equipment/automation/process design, fabrication, and troubleshooting. Primary representative during vendor management, development, and approval of User Requirement Specifications (URS) of major manufacturing equipment identification and procurement. Perform periodic review of manufacturing equipment with Production and Facility personnel to identify areas for obtaining improved operational efficiencies.
Key Duties
  • Process Management
    • Owner of periodic reviews of maintenance and validation activities for major production equipment to identify process improvement and efficiency projects. Includes review and data analytics of complex manufacturing systems.
    • Lead cross-functional teams to ensure production equipment maintains design requirements and meets operational goals and user needs.
    • Manages the URS, FAT, and SAT process for new production equipment.
  • Equipment procurement
    • Mentors and assists other Engineers in the identification and procurement of manufacturing equipment and automation
  • Ensures completion of design documentation (URS, FAT, and SAT) for new equipment procurement according to internal procedures and in accordance with industry standards (GAMP, ASTM E2500)
  • Identifies, qualifies, and works with equipment vendors.
  • Leads cross functional procurement team.
  • Performs project management activities to ensure projects are on time, within budget, and successful.
  • Validation
    • Supports validation engineers for equipment qualification.
    • Author, obtain appropriate approvals, and perform validation studies.
  • Maintenance
    • Support maintenance staff to service equipment as needed.
    • Supplies troubleshooting support to help identify the causes of product/production related problems.
    • Design and implement process improvements and corrective actions.
  • Process Design
    • Designs full-scale manufacturing equipment and/or processes for new products from R&D
  • General
    • Read, understand, and comply with Good Manufacturing Practices and Standard Operating Procedures and accurately complete all required documentation per SOP requirements.
    • Perform all duties in accordance with safety rules as well as appropriate industry and regulatory guidelines.
    • Communicates clearly and effectively with department peers, manufacturing personnel, as well as supervisors, managers, and directors.
    • Assist and train employees on proper equipment operation.
    • Write and/or modify manufacturing and equipment related procedures as needed.
    • Update and maintain facility maps.
    • Other duties as assigned.

Qualifications
  • A minimum of four years of experience in equipment procurement and/or process design.
  • Previous experience in and FDA regulated production environment is desirable
  • Must possess a working knowledge of the Metric System
  • Advanced computer skills required (Word, Excel, CAD knowledge, PLC Database).
  • Proficient in CAD. Solidworks and AutoCard experience preferred.
  • Proficient in programming, specifically industrial control systems and ladder logic. RSLogix 5000 preferred.
  • Thorough knowledge of electrical control systems.
  • Proficient mechanical skills using diagnostic tools used to test, troubleshoot, and repair complex equipment.
  • Ability to read/understand blueprints, schematics, wiring diagrams and other specialized documentation.
  • Ability to read, understand and follow all company Standard Operation Procedures (SOPs) and guidelines.
  • Adhere to safety SOPs and report potential safety hazards.
  • Must have strong math skills.
  • Must be a self-starter, detail oriented, organized, and able to perform under pressure in a fast-paced environment with minimal supervision.
  • Excellent interpersonal, organizational, written, and oral communication skills.
  • Ability to maintain regular attendance and punctuality requirements.
  • Must be able to work overtime and weekends to support production efforts as needed.
  • Must be able to work independently as well as collaboratively in a team setting with peers in a cross functional setting.
  • Excellent analyzing, problem solving and troubleshooting skills