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Sr Validation Engineer Jobs Near Me

Deloitte

System Test and Validation Lead

Columbus, OH · On-site +1

Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Deloitte

System Test and Validation Lead

Columbus, OH · On-site +1

Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Deloitte

System Test and Validation Lead

Columbus, OH · On-site +1

Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Safelite Group, Inc.

Senior Integration Engineer

Columbus, OH · On-site

$100K - $138K/yr

Using a variety of testing tools, the Senior Integrations Engineer needs to test and validate integration solutions to ensure that they work as expected. * The Senior Integrations Engineer needs to ...

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Veeva LIMS SME Consultant / Senior Validation Engineer

Spadtek Solutions LLC

Columbus, OH • On-site

Other

Posted 2 days ago

New

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.

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