ZipRecruiter

Log In

1

In Lims Validation Jobs Near Me

Owens Corning

Sr Technician

Granville, OH · On-site

Leads validation, implementation, documentation and continuous improvement of various laboratory ... Versed in LIMS implementation and utilization. About Owens Corning Owens Corning is a branded ...

Owens Corning

Sr Technician

Granville, OH · On-site

Leads validation, implementation, documentation and continuous improvement of various laboratory ... Versed in LIMS implementation and utilization. About Owens Corning Owens Corning is a branded ...

All JobsIn Lims Validation JobsIn Lims Validation Jobs Near Me

In Lims Validation information

See salary details

$22

$51

$78

How much do in lims validation jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for in lims validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What are popular job titles related to In Lims Validation jobs?

For In Lims Validation jobs, the most frequently searched job titles are:

What job categories do people searching In Lims Validation jobs look for?

The top searched job categories for In Lims Validation jobs are:

What cities are hiring for In Lims Validation jobs?

Cities with the most In Lims Validation job openings:

What states have the most In Lims Validation jobs?

States with the most job openings for In Lims Validation jobs include:

In Lims Validation jobs near you
A map of the United States highlighting the number of In Lims Validation job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of In Lims Validation job openings in each state, with California having the most at 2 and Hawaii the least at 0.

Veeva LIMS SME Consultant / Senior Validation Engineer

Spadtek Solutions LLC

Columbus, OH • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

Title : Veeva LIMS SME Consultant / Senior Validation Engineer

Location: Columbus, OH – Onsite

Job Description:

We are seeking an experienced Veeva LIMS SME Consultant / Senior Validation Engineer to support a Veeva LIMS implementation and validation activities within a GxP-regulated environment.

The ideal candidate will have strong hands-on experience with Veeva LIMS, Computer System Validation (CSV)/Computer Software Assurance (CSA), and pharmaceutical/biotechnology validation practices.

Responsibilities:

  • Lead/support Veeva LIMS implementation and validation activities throughout the system lifecycle, from requirements and design through testing, deployment, and validation closeout.

  • Develop and/or review validation deliverables including URS, risk assessments, validation plans, test scripts, traceability matrices, validation summary reports, and SOPs.

  • Partner with Quality, Laboratory, IT, Business Process Owners, and system stakeholders to define requirements and ensure compliance with business and regulatory needs.

  • Support Veeva LIMS configuration, functional testing, integration testing, UAT, and defect resolution.

  • Apply risk-based CSV/CSA principles and applicable GxP requirements to maintain the validated state of the system.

  • Support data migration, interfaces, integrations, and related systems as part of the LIMS implementation.

  • Participate in change control, deviations, CAPAs, periodic reviews, and other system lifecycle activities.

  • Provide technical and validation expertise during implementation meetings, workshops, testing activities, and issue resolution.

  • Ensure compliance with GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity principles.

  • Support inspection and audit readiness by ensuring complete, accurate, and traceable validation documentation.

Required Qualifications:

  • Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related technical discipline.

  • 5+ years of experience in CSV, CSA, quality, or validation engineering within pharmaceutical, biotechnology, or other GxP-regulated environments.

  • Hands-on Veeva LIMS implementation, validation, or lifecycle management experience is required.

  • Strong understanding of CSV/CSA methodologies, GxP requirements, risk-based validation, and data integrity.

  • Experience developing and executing validation/testing documentation.

  • Strong knowledge of 21 CFR Part 11, EU Annex 11, and GAMP 5.

  • Strong project management, organizational, communication, and problem-solving skills.

  • Must be willing to work onsite in Columbus, OH.

Apply