Global Pharma PM: Regulatory & Supply Chain Transformation

Sii Poland; Lublin; On-site; PLN 180,000 - 320,000; Full time

Benefits offered by this job

Great Place to Work

Centre of internal trainings

Profit sharing

Medical care

Many experts you can learn from

Open and accessible management team

Job summary

Sii Poland seeks an experienced Project Manager to drive complex pharmaceutical initiatives, including optimizing an Anaplan platform for supply chain planning and implementing a unified Regulatory Affairs platform. The role focuses on delivering a global ecosystem by consolidating eight legacy applications for regulatory document management, publishing, and submission tracking.

You will lead cross-functional teams across regions, ensure GxP compliance, and manage stakeholders and vendors to

Qualifications

• 10+ years of project management experience in multinational pharma environments.
• Strong knowledge of GxP regulations and regulatory document handling.
• Ability to design and implement robust project management frameworks.

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, stakeholders, and external vendors across regions.
• Identify regulatory documents to be migrated and ensure compliance with applicable regulations.
• Resolve issues proactively to maintain project momentum and delivery timelines.
• Engage stakeholders at all levels to secure buy-in and ongoing support.
• Communicate project status, risks, and issues clearly to all stakeholders.

Skills

Project management

Pharma industry

GxP compliance

Stakeholder management

Cross-functional leadership

Communication

Multinational teamwork

English proficiency

Job description

Sii Poland seeks an experienced Project Manager to drive complex pharmaceutical initiatives, including optimizing an Anaplan platform for supply chain planning and implementing a unified Regulatory Affairs platform. The role focuses on delivering a global ecosystem by consolidating eight legacy applications for regulatory document management, publishing, and submission tracking.

You will lead cross-functional teams across regions, ensure GxP compliance, and manage stakeholders and vendors to