Join Natek as a Regulatory Process Coordinator and work for a top global pharmaceutical company!This roles supports Process Directors and Associate Directors in managing key processes and projects. The role focuses on activities related to process implementation, communication, compliance, performance tracking, and inspection readiness. You will collaborate closely with teams across Regulatory Affairs and other functions to ensure smooth execution of process strategies, priorities, and governance, including maintaining and managing current procedural documentation.This is a mid-level position providing support in updating regulatory procedures within the ECMS system, performing administrative tasks such as updating SharePoint Online (SPOL), and preparing reports using Excel and Power BI.Location: Warsaw, Poland (3 days/week in the office)Duration: till the end of March 2026Responsibilities:Collaborate with Process Directors and Associate Directors with enhancement of existing processes and procedural documents.Author and collaborate with SMEs to deliver assigned Job aid and supporting documents and templates.Working with the Process and Regulatory experts, develop, establish, monitor, report and assess global KPIs related to safety and regulatory data reporting.Maintain and continuously improve key customer facing service solutions for Process guidance and document access (such as SPOL sites, portals for tickets, Q&A etc).Coordinate specific tasks related to procedural document management to provide oversight to the regulatory process teamUsing understanding of Regulatory processes and regulations to provide support to regulatory process teamIdentify opportunities to improve and simplify the methodology in processes and guidance, provide practical solutions and drive to implementation. Identify issues and risks in own area of work and propose options to mitigate them.Ensure that appropriate, up-to-date records are maintained for complianceSupport activities for GVP, GCP, GRP and GMP audits/inspectionsSupport Delivery of improvement project assignments supporting the business,Building relationships with stakeholders and customers to support pharmacovigilance and regulatory activities and responsibilities including successful partnershipWorking collaboratively to provide expertise and sharing best practices across all regions and in all partnershipsRequirements:Strong administrative skills, including SharePoint Online expertiseExperience working cross-functionally and across culturesExcellent written and verbal communication skills in English (min. B2 level)Good attention to detailUnderstanding or experience in the regulatory areaExperience working with documents that follow formal workflowsAbility to create and manage SharePoint ListsTechnical skills: Power Apps, SharePoint Online (SPOL), AI tools/solutions (e.g., Copilot, ChatGPT, AI Agents)MS Office tools: Excel, SharePoint, PowerApps, AI toolsSoft skills: Collaborative and able to work effectively in an international team, calm, organised, detail-oriented and reliable Desirable:Degree in Science/Pharmacy/Nursing fieldKnowledge of Regulatory operating model and organisationExperience of working in a global organisation, preferably within the pharmaceuticals industry, and of the drug development life cycle and commercial aspects of the industryExperience of working with Procedural documentsBenefits:Internal Mobility Program – enjoy many opportunities for career growth, job rotations, diversity of projects & technologiesReferral Program – enjoy cooperation with your colleagues and get a bonus!5/10 Years NATEK Club – we offer long-term cooperation and celebrate each fifth- year cooperation anniversary with giftsNATEK CSR Events & team buildings – enjoy our values: accountability, partnership and expertise and #workITwithusCafeteriaMedical HealthcareMultisport Club CardTechnical and Personal trainingLanguage coursesOnly for COWLife insuranceBonuses for Personal EventsDay off for volunteering