
Sii · Łódź, Białystok, Bydgoszcz, Kraków, Katowice, Lublin, Poznań, Rzeszów, Szczecin, Toruń
Senior Project Manager - Pharma nad Regulatory Affairs (f/m/x)
W skrócie
zdania wybrane z oferty- 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.
- At least 10 years of proven project management experience within complex, multinational environments
- Managing the implementation of enterprise platforms supporting Regulatory Affairs and Supply Chain operations
Technologie
Pełny opis
z justjoin.itWe 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 escalate, 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 requirements
Relevant project management certifications such as PMP or PRINCE2 are preferred
Treść ogłoszenia pochodzi z justjoin.it i należy do jego autora.
Historia oferty
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- Opublikowana na justjoin.it