Senior Project Manager - Pharma nad Regulatory Affairs (f/m/x)

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

Benefits offered by this job

Great Place to Work

Profit sharing

Centre of internal trainings

Medical care

Job summary

Sii Poland is seeking an experienced Project Manager to lead strategic pharmaceutical projects in a multinational setting. The role focuses on optimizing an Anaplan platform for supply chain planning and implementing a unified Regulatory Affairs platform within a global ecosystem.

You will coordinate cross-functional teams, manage external vendors, and ensure regulatory compliance across regions, driving successful execution and stakeholder alignment.

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.
• Exceptional stakeholder management with influence at all levels.
• Outstanding communication, negotiation, and interpersonal skills.
• Strong analytical and organizational abilities with meticulous attention to detail.
• English fluency at C1 level or higher.

Responsibilities

• Lead complex global projects from initiation through delivery and post-implementation support.
• Manage implementation of enterprise platforms supporting Regulatory Affairs and Supply Chain operations.
• Coordinate cross-functional teams, business stakeholders, and external vendors across regions.
• Identify scope of regulatory documents to migrate, ensure compliance with GxP and regulations.
• Proactively resolve issues to ensure smooth project execution.
• Engage with stakeholders at all levels to secure buy-in and support.
• Communicate project status, risks, and issues to all stakeholders.

Skills

Project management

Stakeholder management

Communication

Negotiation

Interpersonal skills

Analytical thinking

Organizational skills

Job description

We are looking for an experienced Project Manager to join our team, focusing on projects within the pharmaceutical sector. The role involves leading two strategic initiatives: the optimization of an Anaplan platform supporting supply chain planning and the implementation of a unified Regulatory Affairs platform. The larger transformation program aims to consolidate eight existing applications into a single global ecosystem for regulatory document management, publishing, and submission tracking. If you are passionate about leading complex projects in a multinational environment, this opportunity may be the right fit for you.

Your tasks

• Leading complex global projects from initiation through delivery and post-implementation support
• Managing the implementation of enterprise platforms supporting Regulatory Affairs and Supply Chain operations
• Coordinating cross-functional teams, business stakeholders, and external vendors across multiple regions
• Identifying the scope of regulatory documents to be migrated, ensuring compliance with GxP and sector-specific regulations
• Proactively resolving issues before they escalated, ensuring smooth project execution
• Engaging with stakeholders at all levels to ensure project buy-in and support
• Communicating project status, risks, and issues effectively to all stakeholders

Requirements

• At least 10 years of proven project management experience within complex, multinational environments
• Significant expertise in the pharmaceutical industry and a thorough understanding of GxP regulations
• Demonstrated ability to build and implement robust project frameworks from the ground up
• Exceptional stakeholder management skills with the ability to influence at all levels
• Outstanding cultural awareness and sensitivity, with experience working in diverse international teams
• Excellent communication, negotiation, and interpersonal skills
• Strong analytical and organizational abilities, with meticulous attention to detail
• English language proficiency at C1 level or higher

Nice to have

• Relevant project management certifications such as PMP or PRINCE2 are preferred

Job no. JOB-LKZF7

Sii ensures that all hiring decisions are made solely on the basis of qualifications and competence. We are committed to equal and fair treatment of all, regardless of legally protected characteristics. At Sii, we promote a diverse and inclusive work environment, in full compliance with applicable anti-discrimination laws.

Benefits For You

• Great Place to Work
• Solid financial situation
• Contracts with the biggest brands
• Centre of internal trainings
• Many experts you can learn from
• Open and accessible management team
• Profit sharing
• Passion Sponsorship program
• Regular integration events and trips
• Comfortable and well-equipped offices
• MySii app
• Medical care