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Computer Validation Jobs in Kentucky (NOW HIRING)

Validation Specialist Position Summary * Typical working hours are Monday-Friday 8 AM-5 PM * This ... Specific vision requirements include reading of written documents and frequent use of computer ...

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 ...

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 ...

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 ...

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 ...

Essential Duties * Specify and create CAD drawings for custom-fabricated assemblies and ... Communicate and validate design requirements with internal and external customers to ensure ...

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Computer Validation information

See Kentucky salary details

$9

$47

$74

How much do computer validation jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for computer validation in Kentucky is $47.18, according to ZipRecruiter salary data. Most workers in this role earn between $36.35 and $55.96 per hour, depending on experience, location, and employer.

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.

Validation Specialist

Validation Specialist

Catalent, Inc.

Winchester, KY • On-site

Full-time

Life, Retirement, PTO

Posted 21 days ago


Catalent rating

7.7

Company rating: 7.7 out of 10

Based on 49 frontline employees who took The Breakroom Quiz

46th of 71 rated pharmaceutical


Job description

Validation Specialist
Position Summary
  • Typical working hours are Monday-Friday 8 AM-5 PM
  • This position is 100% on-site in Winchester, Kentucky.

Catalent's Winchester location is the flagship US manufacturing location for large scale oral dose forms, with integrated analytical and development services. With 28 years of expertise in product development, technology transfers and commercial manufacturing, and roots in industry-leading Glatt technology.
The Validation Specialists shall provide validation support and oversite of activities in one or more of the following areas; 1) NPIx for new processes and equipment brought into the Catalent facility, 2) Process/Cleaning Validation activities for all Drug Products/APIs being commercialized and/or 3) Equipment Qualification for all new Equipment/Systems, change controls to existing qualified Equipment/Systems and utilities/facility qualifications. The Validation Specialist is an extension of the Supervisor / Sr. Validation Specialist on all validation activities, including drafting and approving documents, execution of protocols on the manufacturing floor, drafting reports, attending customer meetings, supporting customer audits to provide validation support and to ensure they meet manufacturing timelines and to maintain compliance.
The Role
  • Draft protocols and reports for Computerized Systems Validation, and/or Automated Production Equipment Validation, and/or Facility Qualification, and/or Analytical Equipment Validation, and/or Process Validation and/or Cleaning Validation. Responsibilities include developing the appropriate and required protocol documents in accordance with the current site and corporate Validation SOP's and guidelines. Obtaining approval signatures from the Catalent management and as required from customers.
  • Execute approved protocols and coordinate the activities with other departments (e.g. engineering, maintenance, production, etc...) as required.
  • Review and approve site Annual Product reviews.
  • Assists in site NPIx gate reviews.
  • Involvement with customer audits and responding to audit observations and corrective actions.
  • Assist in investigations of manufacturing / facility deviations as asked of by Quality Systems.
  • Addressing process/facility Change Controls issued.
  • Addressing process/facility CAPAs issued.
  • Interacts with customers, including participating in scheduled teleconferences and responding to customer requests/complaints.
  • Other duties as required in support of Catalent Pharma Solutions high performance

The Candidate
  • Bachelor's Degree preferred.
  • Associates degree in life sciences (e.g., Pharmaceuticals, Chemistry, Biology, etc.) or related field required with 2 years experience in the Pharmaceutical/ Biotechnology or Medical Devices industry; OR Experience in authoring, reviewing and approving of validation deliverables including Risk Assessments, Test Plans, Protocols, Reports, Summary Reports and Standard Operating Procedures (SOPs).
  • Scientific writing skills
  • Working knowledge of cGMP guidelines and regulations,
  • Knowledge of validation SOPs and site policies associated to their area.
  • Individual may be required to sit for an extended period of time. Specific vision requirements include reading of written documents and frequent use of computer monitor

Why You Should Join Catalent
  • Several Employee Resource Groups focusing on D&I
  • Tuition Reimbursement - Let us help you finish your degree or earn a new one!
  • Generous 401K match
  • 152 hours accrued PTO + 8 paid holidays

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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