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Wallet icon Coin icon Rate 160 000 CZK - 200 000 CZK / month info

info The reward is calculated upon delivery of 20 MD per month (1MD=8h)

Timer icon Form of cooperation Freelance: Full-time
Briefcase icon Sector Healthcare and Pharmacy
Location icon Location Praha, 80% Remote
Project duration 2 months with possibility of extension
Period of cooperation 01.11.2026 - 31.12.2026
Start date 01.11.2026 or by agreement
Project duration 2 months with possibility of extension
Period of cooperation 01.11.2026 - 31.12.2026
Start date 01.11.2026 or by agreement

Languages

  • English flag English - active, B2/C1/C2

Project description

  • end-to-end delivery of the ASM converter from requirements gathering, through semantic modeling and validation, to release readiness and deployment
  • defining the scope of the converter, Merck Key Fields, scientific requirements, validation strategy, acceptance criteria, and test scenarios
  • leading discovery and working sessions with Scientists, SMEs, and other stakeholders for data collection from laboratory instruments
  • collaboration with Semantic Engineers and vendors on mapping instrument data to the Allotrope Ontology and defining semantic mappings and schema extensions
  • coordinating converter development with vendors and technical teams according to scientific, technical, quality, compliance, and business requirements
  • leading pre-validation activities including data sample review, semantic mapping validation, dry-run ASM assessments, and converter output verification
  • leading and providing expert oversight to the Quality Engineering squad for source-to-target validation, data transformation verification, traceability testing, and converter quality evaluation
  • reviewing validation results, test evidence, defects, and quality metrics to support release readiness
  • leading defect triage, issue resolution, risk assessments, and planning of corrective actions throughout the converter's lifecycle
  • coordinating test reviews, approval workflows, Jira traceability, audit readiness, and release sign-offs
  • creating and revising SDLC documentation, mapping specifications, lifecycle documents, and validation artifacts
  • managing risks and dependencies, and communicating status with Delivery Orchestrators, Product Owners, Business Leads, and other stakeholders
  • leading and mentoring team members and promoting standards for ASM, Allotrope, semantic modeling, validation methodologies, and scientific data quality
  • improving converter quality, validation efficiency, documentation standards, process standardization, and reusable validation artifacts
  • ensuring compliance with Quality Engineering, SDLC, data integrity, data governance, and regulatory compliance requirements

Project requirements

  • advanced experience with:
    • minimum of 6 years of experience in Data Engineering, Data Integration, Data Management, or another data-focused role
    • Data Quality Assurance including defining solution scope, requirements, acceptance criteria, validation approaches, and test scenarios according to business and data requirements
    • leading small technical teams, prioritizing work, removing impediments, and managing execution according to project milestones
  • experience with:
    • collaborating with non-technical stakeholders from business or scientific environments and translating their requirements into scalable data solutions
    • managing and documenting risks, issues, dependencies, decisions, and stakeholder expectations throughout the project
    • collaborating across Business, Scientific SMEs, Engineering, Quality, Product, Architecture, and external vendors
    • facilitation, communication, stakeholder management, and analytical problem-solving
  • advanced knowledge of:
    • data modeling, data mapping, data transformation, data quality, and traceability
  • knowledge of:
    • software lifecycle, data lifecycle management, and data governance
    • university degree in Computer Science, Engineering, Data Science, Information Systems, Biotechnology, or a related field, or equivalent professional experience
  • advantageous:
    • experience in the pharmaceutical industry and drug development process
    • experience with scientific data and laboratory workflows
    • leading data onboarding, integration, validation, migration, or transformation initiatives in a complex business environment
    • experience with Allotrope data schemas, especially the Allotrope Simple Model
    • experience with Jira, VERA, Xray, Confluence, Mural, or automated validation testing tools

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