Hybrid Data Validation Associate — Clinical Systems

MSD; Warszawa; Hybrid; PLN 140,000 - 200,000; Full time

Job summary

Merck & Co., Inc. in Warsaw, Poland, is hiring a Business System Validation Associate Specialist to validate data integration and automation solutions that support clinical and business operations.

The role focuses on CSV, data integrity, and regulatory compliance, with hands-on testing, documentation, and audit-ready summaries. You will plan validation activities, execute tests across data pipelines, log defects, and collaborate with cross-functional teams to ensure timely delivery and

Qualifications

• Bachelor's or higher in life sciences or related field preferred; relevant validation/testing experience required.
• Experience with CSV/CSV-like systems, data integrity checks, and audit-ready documentation.
• Familiarity with clinical data management systems, data integration environments, and regulatory guidelines (GCP, CSV).

Responsibilities

• Plan validation strategies and readiness activities for data integration and automation projects.
• Execute validation tests per protocols; log, track, and retest defects; ensure traceable evidence and audit-ready reports.
• Prepare validation summaries and collaborate with cross-functional teams to ensure compliant delivery.

Skills

Adaptability

Analytical problem solving

Data integrity

Regulatory compliance

CSV validation

Data management

Data analysis

Documentation practices

GxP

Communication

Education

Bachelor's degree in life sciences / related field

Non-Degree with 2+ years experience

Associate's degree (1+ year)

Job description

Merck & Co., Inc. in Warsaw, Poland, is hiring a Business System Validation Associate Specialist to validate data integration and automation solutions that support clinical and business operations.

The role focuses on CSV, data integrity, and regulatory compliance, with hands-on testing, documentation, and audit-ready summaries. You will plan validation activities, execute tests across data pipelines, log defects, and collaborate with cross-functional teams to ensure timely delivery and