Senior GxP IT Project Manager

Galderma Polska Sp. z o.o.; Kraków; Hybrid; PLN 220,000 - 360,000; Full time

Benefits offered by this job

Hybrid work culture

Bonus structure and extended benefits

Ownership and accountability from day

Job summary

Galderma Polska Sp. z o.o.

in Kraków seeks a Senior Project Manager (GxP) to lead planning, execution and governance of complex IT delivery projects in a highly regulated pharmaceutical environment, with a strong focus on GxP compliance, validation, quality, audit readiness and controlled delivery. You will translate compliance expectations into robust project plans, ensure documentation and validation deliverables meet standards, and collaborate with Quality, CSV/validation, IT and external

Qualifications

• 8–10 years of project, programme or transformation management in GxP-regulated settings.
• Deep understanding of GxP, including computer system validation and data integrity.
• Bachelor’s or Master’s degree in a relevant field.

Responsibilities

• Lead planning, implementation and delivery of complex IT projects in GxP-regulated environments.
• Coordinate multiple interrelated projects with GxP impacts and validation dependencies.
• Ensure delivery aligns with methodologies, governance, budgets, timelines, GxP expectations and quality procedures.
• Drive validation artefacts: strategy inputs, risk assessments, requirements docs, test evidence, traceability, approvals and controlled release docs.
• 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, data integrity or audit readiness.

Skills

GxP PM

Validation

Data integrity

Stakeholder mgmt

Quality Assurance

Leadership

Education

Bachelor/Master in a relevant field

Job description

Galderma Polska Sp. z o.o.

in Kraków seeks a Senior Project Manager (GxP) to lead planning, execution and governance of complex IT delivery projects in a highly regulated pharmaceutical environment, with a strong focus on GxP compliance, validation, quality, audit readiness and controlled delivery. You will translate compliance expectations into robust project plans, ensure documentation and validation deliverables meet standards, and collaborate with Quality, CSV/validation, IT and external