GxP IT Project Lead — Regulated Pharma, Kraków

Galderma; Kraków; Hybrid; PLN 140,000 - 190,000; Full time

Benefits offered by this job

Hybrid work culture

Competitive compensation with bonus

Diversity and inclusion

Career path development

Ownership and accountability

Job summary

Galderma Krakow is seeking a Senior Project Manager (GxP) to lead planning, execution and governance of complex IT delivery projects in a highly regulated pharmaceutical environment. The role focuses on GxP compliance, validation, quality, audit readiness and controlled delivery.

You will translate compliance expectations into robust project plans, ensure documentation and validation deliverables, and collaborate with Quality, CSV/validation, IT and external partners throughout the lifecycle.

Qualifications

• 8-10 years of experience in project, programme or transformation management in life sciences/pharma or similarly regulated environments.
• Deep understanding of GxP principles and regulated delivery expectations, including validation, data integrity and traceability.

Responsibilities

• Lead the planning, implementation and governance of complex IT projects in GxP-regulated environments.
• Coordinate multiple interrelated projects with validation dependencies, quality risks and regulatory commitments.
• Ensure delivery aligns with governance standards, budgets, timelines, GxP and quality procedures.
• Drive validation artefacts: validation strategy inputs, risk assessments, requirements, test evidence and traceability.
• Partner with Quality, CSV/validation, IT and external providers for compliant delivery from initiation to handover.
• Maintain inspection-ready project documentation and address gaps impacting validation or data integrity.

Skills

Leadership

Project management

Quality/compliance

Regulated IT delivery

Analytical thinking

Education

Bachelor's or Master's degree in a relevant field

Tools

CSV/Validation tools

Job description

Galderma Krakow is seeking a Senior Project Manager (GxP) to lead planning, execution and governance of complex IT delivery projects in a highly regulated pharmaceutical environment. The role focuses on GxP compliance, validation, quality, audit readiness and controlled delivery.

You will translate compliance expectations into robust project plans, ensure documentation and validation deliverables, and collaborate with Quality, CSV/validation, IT and external partners throughout the lifecycle.