Global Validation Specialist – Master Data

Boehringer Ingelheim Pharmaceuticals, Inc.

Wrocław

On-site

PLN 120,000 - 180,000

Full time

7 days ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

Boehringer Ingelheim Pharmaceuticals, Inc. in Wrocław is seeking a Validation Specialist to map and optimize the GBS Enabling Services' validation processes.

You will coordinate change requests, perform impact analyses, review documents, and ensure systems stay in a validated state within an agile, cross-functional team. The role requires 2–4 years in Validation Management (CSV) or a tightly regulated quality role, a Bachelor’s degree, and fluent English.

Qualifications

  • 2–4 years of experience in Validation Management, ideally in CSV, or in a quality role in a regulated environment.
  • Bachelor's Degree; engineering, sciences, pharmaceuticals or biotechnology preferred.
  • Knowledge of GxP regulations is advantageous.
  • Experience with Master Data or Reference Data is an asset.
  • Experience with Test and Change Management is a plus.
  • Experience with Agile methods (SCRUM, Kanban) and JIRA is beneficial.

Responsibilities

  • Coordinate activities around change requests and impact analyses.
  • Review and approve validation documents and ensure a validated state of systems.
  • Support daily operation of processes and applications.
  • Ensure processes and systems are compliant and validated.
  • Manage testing activities and documentation.
  • Apply Agile methods and participate in projects driven by this methodology.

Skills

Analytical thinking
Problem solving
Communication
Team player
Organizational skills

Education

Bachelor's Degree in engineering/sciences/pharma/biotech

Tools

JIRA

Job description

Boehringer Ingelheim Pharmaceuticals, Inc. in Wrocław is seeking a Validation Specialist to map and optimize the GBS Enabling Services' validation processes.

You will coordinate change requests, perform impact analyses, review documents, and ensure systems stay in a validated state within an agile, cross-functional team. The role requires 2–4 years in Validation Management (CSV) or a tightly regulated quality role, a Bachelor’s degree, and fluent English.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Validation Specialist (Master Data Management, fixed-term contract)
Validation Specialist (Master Data Management, fixed-term contract)

our future Intern • Wrocław

On-site
PLN 120,000 - 180,000
Senior Data Steward: Data Quality & Governance
Senior Data Steward: Data Quality & Governance

Boehringer Ingelheim Pharmaceuticals, Inc. • Wrocław

On-site
PLN 180,000 - 260,000
Hybrid Data Validation Associate — Clinical Systems
Hybrid Data Validation Associate — Clinical Systems

MSD • Warszawa

Hybrid
PLN 140,000 - 200,000
Hybrid: Data Validation & Compliance Specialist
Hybrid: Data Validation & Compliance Specialist

MSD • Warszawa

Hybrid
PLN 90,000 - 130,000
Senior Specialist, Technical Product Complaints (GMP)
Senior Specialist, Technical Product Complaints (GMP)

Boehringer Ingelheim Pharmaceuticals, Inc. • Wrocław

Hybrid
PLN 90,000 - 130,000
GxP Data Platform Validation Lead (Warsaw)
GxP Data Platform Validation Lead (Warsaw)

Xebia Group • Województwo mazowieckie

On-site
PLN 90,000 - 150,000
Senior Validation Lead - Data Integration & Automation
Senior Validation Lead - Data Integration & Automation

MSD Polska • Województwo mazowieckie

Hybrid
PLN 180,000 - 300,000
Hybrid work arrangement
Professional development programs
Senior Serialization & Validation Analyst (GxP Expert)
Senior Serialization & Validation Analyst (GxP Expert)

Galderma S.A. • Kraków

On-site
PLN 180,000 - 240,000
Private healthcare
Life insurance
Pension plan
+4
Master Data Management Process Specialist (SAP Solution Testing)
Master Data Management Process Specialist (SAP Solution Testing)

Boehringer Ingelheim Pharmaceuticals, Inc. • Wrocław

On-site
PLN 120,000 - 160,000
Global IT Quality & Validation Specialist
Global IT Quality & Validation Specialist

Bayer AG • Województwo pomorskie

On-site
PLN 90,000 - 120,000
Top locations