6424 - Lead Validation Engineer (Data Lake) / CSV Engineer
Verista, Inc.
| Company | Verista, Inc. |
| Category | Engineering |
| Location | Conshohocken |
| Remote | On-site (inferred) |
| Employment | Not stated |
| Level | Lead |
| Salary | Not stated by the employer |
| Posted | 26 Jun 2026 |
| Last verified | 30 Jul 2026 |
| Source | Employer career page (greenhouse) |
Description
Description
Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
We empower and support our colleagues
We commit to client success at every turn
We have the courage to do the right thing
We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
We constantly acquire new skills and learn from our experiences to enhance our collective expertise
Validation Engineer (Data Lake) Responsibilities:
Qualification Strategy & Validation Leadership
Lead qualification activities for an enterprise cloud-based Data Lake platform using modern, risk-based CSA methodologies.
Assess the current architecture, existing validation deliverables, and identify opportunities to simplify and modernize qualification activities while maintaining compliance.
Develop and implement a scalable qualification model supporting future onboarding of GxP systems, data sources, interfaces, and pipelines.
Establish sustainable validation and governance procedures supporting both GxP and non-GxP use cases.
Validation Planning & Documentation
Author and maintain:
Data Lake Validation Plan
Requirements Specifications
Technical Specifications and As-Built Configuration Documentation
Infrastructure Qualification (IQ) Protocols
Operational Qualification (OQ) Protocols
Validation Summary Reports
Test Summary Reports
Develop sustainable documentation approaches that leverage platform automation and minimize unnecessary documentation.
Testing & Verification
Define streamlined testing strategies focused on critical infrastructure and business processes.
Facilitate and coordinate testing activities executed by the Data and Infrastructure teams.
Implement targeted verification approaches aligned with CSA principles.
Ensure validation deliverables support ongoing lifecycle management and change control.
Governance & Lifecycle Management
Develop and implement governance procedures for the enterprise data platform.
Establish change control processes supporting:
GxP data source onboarding
Data pipeline qualification
Interface assessments
Ongoing platform enhancements
Develop Data Lake Administration SOPs and associated work instructions.
Support implementation and governance of Power BI solutions used for GxP business processes.
Compliance & Risk Management
Ensure alignment with:
GAMP 5 Second Edition
Computer Software Assurance (CSA) guidance
21 CFR Part 11
EU GMP Annex 11
Data Integrity requirements
Good Documentation Practices (GDP)
Leverage supplier assessments, cloud platform controls, and risk-based verification methodologies.
Requirements:
Bachelor's degree in Computer Science, Engineering, Information Systems, Life Sciences, or related discipline.
8+ years of Computer System Validation (CSV), CSA, or IT Compliance experience within pharmaceutical, biotechnology, or regulated environments.
Strong experience qualifying cloud-based platforms and infrastructure.
Demonstrated experience implementing risk-based CSA methodologies.
Deep understanding of:
GAMP 5 Second Edition
FDA CSA Guidance
21 CFR Part 11
EU Annex 11
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