Global Pharma PM Lead: Regulatory & Supply Chain

Sii Poland; Toruń; On-site; PLN 180,000 - 260,000; Full time

Benefits offered by this job

Profit sharing

Medical care

Internal trainings

Job summary

Sii Poland is seeking an experienced Project Manager to lead two strategic initiatives in the pharmaceutical sector: optimizing an Anaplan platform for supply chain planning and implementing a unified Regulatory Affairs platform. The larger program aims to consolidate eight existing applications into a single global ecosystem for regulatory document management, publishing, and submission tracking.

If you excel at steering complex multinational projects and engaging diverse stakeholders, this is

Qualifications

• At least 10 years of proven project management experience in multinational environments.
• Significant expertise in the pharmaceutical industry and GxP regulations.
• Ability to build and implement robust project frameworks from the ground up.
• Excellent stakeholder management and ability to influence at all levels.
• Strong communication and organizational skills; English C1+.

Responsibilities

• Lead complex global projects from initiation through delivery and post-implementation support.
• Manage the implementation of enterprise platforms for Regulatory Affairs and Supply Chain.
• Coordinate cross-functional teams, stakeholders, and external vendors across multiple regions.
• Identify the scope of regulatory documents to be migrated, ensuring compliance with GxP and sector-specific regulations.
• Proactively resolve issues before they escalate, ensuring smooth project execution.
• Engage with stakeholders at all levels to ensure project buy-in and support.
• Communicate project status, risks, and issues effectively to all stakeholders.

Skills

Project management

Stakeholder management

Pharma industry knowledge

GxP regulations

Cross-functional leadership

Job description

Sii Poland is seeking an experienced Project Manager to lead two strategic initiatives in the pharmaceutical sector: optimizing an Anaplan platform for supply chain planning and implementing a unified Regulatory Affairs platform. The larger program aims to consolidate eight existing applications into a single global ecosystem for regulatory document management, publishing, and submission tracking.

If you excel at steering complex multinational projects and engaging diverse stakeholders, this is