The Technical Project Manager will lead project planning, manage resources, track project compliance, oversee budgets, and report on project progress, ensuring quality standards are met.

The Senior Executive - QA oversees quality management, supplier quality assurance, documentation control, compliance with regulations, validation, and training programs, ensuring product quality and GMP adherence.

The Manager Biosimilars Analytics oversees development and execution of analytical strategies for biosimilars, ensuring regulatory compliance and effective collaboration with partners. They provide expert advice and lead complex projects to meet biosimilar strategy goals.

Manage quality control activities in the microbiology laboratory, ensuring adherence to regulations. Oversee analyses, validations, and team training while maintaining safety standards.

Manage inventory data and financial reporting for Group consolidation. Oversee audits and provide support for local financial teams, ensuring compliance with policies.

The P&O Operational Partner will support HR processes in Poland, manage employee records, handle onboarding and offboarding, and ensure compliance with labor laws.

Lead sourcing activities and negotiate with suppliers, manage procurement data, track cost savings, and collaborate with stakeholders to support business continuity.

As an Artwork Specialist, you will design packaging graphics, ensuring accuracy, collaborating with teams, and validating print proofs following guidelines.

The Global Procurement COE Head leads procurement strategies, governance, and transformation efforts, driving cost optimization, compliance, sustainability, and cross-functional stakeholder engagement.

Manage and oversee the corporate Quality Management System (QMS) across all operations, ensuring compliance with regulatory standards and continuous improvement of quality processes. Lead the development, implementation, and lifecycle management of QMS, along with training and audit participation.

Ensure quality lifecycle management of product portfolios, oversee operational quality, manage audits, and monitor KPIs while collaborating with stakeholders.

The QA Specialist ESO manages quality operations for a product portfolio, overseeing audits, compliance, change controls, and documentation, ensuring adherence to regulations.

The Executive – QC, Microbiology will conduct microbial analyses, maintain laboratory practices, and ensure compliance with GMP/GLP standards while coordinating activities with production.

The Business Development Manager will identify clients, build relationships, negotiate contracts, and support sales of proprietary APIs for Zentiva's API CDMO activities.

Responsible for operational quality management, auditing, KPI monitoring, compliance evaluations, and support during product launches for a dedicated product portfolio.

The role involves leading global engineering initiatives, focusing on operational excellence, sustainability, and team development across pharmaceutical manufacturing sites.

The Business Intelligence Analyst will optimize data processes, implement ETL solutions, and create analytical tools for maximizing data insights within the organization.

The Junior Registration Specialist will lead regulatory activities for new projects, ensuring timely submission and compliance with regulatory standards, while managing documentation and communication with regulatory authorities.

The Procurement Category Manager develops and executes procurement strategies, manages supplier negotiations, and ensures integration across business units while delivering savings and compliance.

The role involves characterizing active substances, conducting stress tests, developing chromatography methods, and contributing to product development in a pharmaceutical R&D setting.