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6 дней назад

Senior Data Migration Technical Analyst (GxP)

Формат работы
remote (только Costa_rica)/onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
CR
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Senior Data Migration Technical Analyst (GxP): Leading end-to-end data migration for regulated pharmaceutical and biotechnology systems with an accent on source-to-target mapping, transformation, reconciliation, and audit-ready traceability. Focus on designing repeatable migration pipelines, validating data integrity, and managing cutover, rollback, and post-migration stabilization across GxP environments.

Location: Costa Rica, Heredia; work from home 100% of the time or work from one of the global offices

Company

hirify.global is a global engineering firm delivering custom software, AI agent deployments, data platforms, cloud migrations, systems integration, and application modernization.

What you will do

  • Lead data migration workshops, source-data inventory, profiling, and migration-scope definition.
  • Create and maintain approved source-to-target mappings, cleansing rules, transformation logic, load sequences, and exception rules.
  • Develop extracts, transformation scripts, import files, and repeatable migration runs.
  • Reconcile source and target data using control totals, field comparisons, relationship checks, exception reporting, and risk-based sampling.
  • Maintain traceability across extraction, transformation, staging, loading, testing, and final verification.
  • Plan cutover, rollback, data freezes, and post-migration stabilization while collaborating with QA, CSV, IT, vendors, and business stakeholders.

Requirements

  • 5+ years of experience with R in data migration, data conversion, system implementation, data integration, or enterprise content migration.
  • Experience completing a full migration lifecycle from source discovery through production cutover and reconciliation.
  • Strong SQL, relational database, ETL or scripted transformation, data-quality, source-to-target mapping, and reconciliation skills.
  • Experience in a pharmaceutical or biotechnology GxP environment with knowledge of GAMP 5, 21 CFR Part 11, CSV or CSA, and ALCOA+ principles.
  • Strong analytical, documentation, communication, and problem-solving skills with excellent verbal and written English.
  • Ability to investigate migration defects and document exceptions, resolutions, metadata, identifiers, dependencies, and relational integrity.

Nice to have

  • LabWare LIMS or LabWare SaaS experience, including laboratory, QA/QC, specifications, methods, products, samples, results, stability, or environmental-monitoring data.
  • Experience with LabWare LIMS, Egnyte, Veeva Vault, or ZenQMS.
  • Experience migrating controlled documents, training records, quality records, metadata, permissions, audit trails, electronic signatures, or version history.
  • Experience with Python, PowerShell, SQL Server, Oracle, PostgreSQL, REST APIs, or Databricks.

Culture & Benefits

  • Work from home full-time or use a global office.
  • Supportive engineering and project-management colleagues in a collaborative environment.
  • Generous vacation schedule.
  • New laptop and additional benefits.

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