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# Assay Data Management Specialist

- **Company:** EUROFINS
- **Location:** Spring House, PA, United States
- **Contract:** Permanent contract
- **Skills:** Data Analysis, Customer Data Management, Product Software Implementation Methods, Information Technology, Data Management
- **Published:** October 1, 2026
- **Apply:** https://jobs.smartrecruiters.com/Eurofins/744000152750459-assay-data-management-specialist

## About the Role

* Bachelor's degree in a scientific, technical, data management, or related field with at least 3-5 years of industry experience, or an M.S. degree with 1-3 years of related experience.
 * Experience in bioanalysis, laboratory operations, scientific data management, laboratory informatics, or a related field.
 * Demonstrated ability to understand scientific workflows and translate them into practical template, data-capture, or data-management requirements.
 * Experience collaborating across scientific, data management, technical, and project teams.
 * Strong organizational skills with the ability to manage multiple concurrent projects and deliverables.
 * Strong written and verbal communication skills.
 * Highly detail-oriented with a focus on accuracy, consistency, quality, and successful implementation.
 * Ability to work independently while effectively collaborating within cross-functional teams.

Preferred skills

 * Experience with Benchling or similar scientific data management platforms.
 * Experience supporting bioanalytical or laboratory assay onboarding.
 * Experience with both manual and automated/robotic assay workflows.
 * Experience building or configuring templates, assay preparations, workflows, or similar scientific data-management components.
 * Experience working collaboratively with scientists, data management professionals, IT, and other technical teams.
 * Familiarity with requirements specifications and translating requirements into functional project deliverables.
 * Experience developing test cases and UAT scripts and participating in UAT activities.
 * Experience working in a regulated or quality-focused laboratory environment.
 * Familiarity with scientific data-management or software implementation lifecycles.
 * Experience supporting process standardization or continuous improvement activities.

## Description

* Embed within the data management and project teams supporting the onboarding and implementation of new bioanalytical assays.
 * Partner with scientists and subject matter experts to understand assay workflows, rules, calculations, data requirements, and execution processes.
 * Gather, clarify, organize, and document scientific and operational requirements needed to support assay execution, data capture, and data analysis.
 * Develop and configure templates and assay preparations required to support assay execution, data capture, and analysis.
 * Support both manual and automated/robotic assay implementations.
 * Participate throughout the end-to-end template development lifecycle, from requirements gathering and documentation through configuration, testing, implementation, and refinement.
 * Review and interpret applicable requirements specifications to ensure requirements are appropriately reflected in templates and project deliverables.
 * Compare requirements and workflows across assays and projects to identify gaps, differences, and opportunities for standardization.
 * Collaborate with scientists, data management, IT, and other stakeholders to translate scientific and operational requirements into effective assay-supporting solutions.
 * Develop sufficient understanding of assay-specific rules and workflows to identify expected template behavior, potential gaps, and appropriate test scenarios.
 * Prepare test cases and UAT scripts throughout the template development process and participate in UAT, including documenting and resolving identified issues.
 * Confirm that templates, assay preparations, and related deliverables accurately support intended assay workflows and data requirements.
 * Maintain appropriate documentation of requirements, decisions, configurations, testing activities, and project deliverables.
 * Support multiple assay projects simultaneously and identify opportunities to improve consistency, efficiency, usability, and quality across assay onboarding activities.
 * Assist with interpretation of clinical protocols to accurate data entry during study design