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Veeva Implementation Jobs Near Me

Merck & Co.

Specialist Technical Writing

New Albany, OH · On-site

$70 - $100/hr

B.S. 2+ YOE would be ideal, previous Veeva experience, and prior deviation and CAPA experience ... Track pending activities required to support change control implementations. * Liaise with Quality ...

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As of Aug 26, 2026, the average yearly pay for veeva implementation in the United States is $112,486.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,000.00 and $141,000.00 per year, depending on experience, location, and employer.

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A map of the United States highlighting the number of Veeva Implementation job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Veeva Implementation 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 1 day ago. 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