Senior Project Manager - Global Pharma Transformation Lead

Sii Poland; Poznań; On-site; PLN 210,000 - 270,000; Full time

Benefits offered by this job

Medical care

Centre of internal trainings

Profit sharing

Open management team

Great Place to Work

Job summary

Sii Poland is seeking an experienced Project Manager to lead complex pharmaceutical programs in a multinational environment. You will oversee the optimization of an Anaplan platform for supply chain planning and drive the implementation of a unified Regulatory Affairs platform.

The role aims to consolidate eight existing applications into a single global ecosystem for regulatory document management, publishing, and submission tracking, requiring strong leadership and cross-functional

Qualifications

• 10+ years of proven project management experience in multinational environments.
• Significant pharma industry experience with GxP regulations.
• Ability to build and implement robust project frameworks from the ground up.
• Strong stakeholder management and cross-functional collaboration skills.
• Excellent communication and negotiation abilities; English at C1+.

Responsibilities

• Lead complex global projects from initiation through delivery and post-implementation support.
• Oversee the implementation of enterprise platforms for Regulatory Affairs and Supply Chain operations.
• Coordinate cross-functional teams, business stakeholders, and external vendors across regions.
• Define scope of regulatory documents to be migrated, ensuring GxP compliance.
• Proactively resolve issues to keep projects on track.
• Engage stakeholders at all levels to ensure buy-in and support.
• Communicate project status, risks, and issues clearly to all stakeholders.

Skills

Project management

Stakeholder management

GxP knowledge

Cross-functional coordination

Communication

Analytical thinking

English proficiency

Job description

Sii Poland is seeking an experienced Project Manager to lead complex pharmaceutical programs in a multinational environment. You will oversee the optimization of an Anaplan platform for supply chain planning and drive the implementation of a unified Regulatory Affairs platform.

The role aims to consolidate eight existing applications into a single global ecosystem for regulatory document management, publishing, and submission tracking, requiring strong leadership and cross-functional