Lead deployment of Lean 4.0 across production, quality, and labs; coach leaders and teams; run Tier Management, Standard Work, VSM, and Kaizen events; use digital tools and data to identify improvements; collaborate with Quality/Operations and consultants to drive sustained performance and culture change.

The Senior Lead Scientist will assess API suppliers, conduct analytical testing, lead method transfers, and interface with teams to ensure compliance and efficiency in drug development processes.

The Epidemiology Lead is responsible for developing and executing epidemiology strategies throughout the product lifecycle, ensuring evidence generation for clinical development and market access, collaborating with teams, and applying advanced analytic techniques.

The Manager, Project Engineering is responsible for overseeing capital projects, collaborating with multiple departments, and ensuring compliance with quality and safety practices.

Own end-to-end Polish payroll processing: collect and validate inputs, reconcile outputs, coordinate with HR, Finance and external vendor, ensure legal compliance, respond to employee payroll inquiries, prepare statutory filings, and support continuous improvement and payroll projects.

The Senior Quality Director oversees quality operations, ensuring compliance with regulatory standards and leading quality management initiatives to ensure product quality.

The Director of Regulatory Compliance will establish and lead the Global Regulatory Affairs Compliance function, ensuring adherence to regulatory processes, managing audits, and evolving the Quality Management System while collaborating with cross-functional teams.

Develop and execute marketing strategies for assigned pharmaceutical brands, manage A&P budgets and forecasts, support new product evaluation and market development, prepare demand and sales forecasts, and contribute to long-range pricing, volume and profit planning.

Manage and publish regulatory dossiers for product submissions, ensuring compliance and quality control while mentoring junior staff. Act as a subject matter expert for publishing activities.

The QC Analyst will conduct testing of materials and products, drive KPI achievement, update documentation, troubleshoot methods, engage in projects, and maintain equipment care.

The Intern, R&D Bioanalytical will support the Bioanalytical laboratory by operating equipment, preparing solutions and samples, and assisting with record-keeping.

The Pharmacovigilance Officer ensures compliance with pharmacovigilance obligations, reviews agreements, liaises with stakeholders, negotiates agreements, and maintains audit readiness.

The Pricing Manager develops pricing strategies and maximizes reimbursement for the company's portfolio in the Czech Republic, collaborating with cross-functional teams and ensuring compliance with regulations.

Support and implement continuous improvement initiatives site-wide by analysing data and processes, presenting prioritized recommendations, coaching stakeholders on OE methodologies (Lean, Six Sigma, TPM), delivering workshops, and driving improvements focused on safety, quality, cost and delivery.

The Senior Director will lead US regulatory strategies for advertising and promotions, manage compliance with regulations, and communicate with stakeholders to mitigate regulatory risks.

The Pricing Coordinator will develop and manage pricing policies, analyze pricing strategies, ensure regulatory compliance, and lead pricing-related projects in the pharmaceutical sector.

The Quality Assurance Supervisor will coordinate and oversee Product Quality Review and Continued Process Verification reports, ensuring compliance with procedures. They will manage the QA team, facilitate work efforts, and ensure timely report preparations to support manufacturing schedules.

The QA Officer supports the QA team with GDP processes, product quality, and administrative tasks, including document screening and corrective actions.

The Senior Specialist, QA Quality Systems leads quality system investigations, manages CAPA actions, and supports audits in compliance with pharmaceutical regulations.

The Labelling Hub Manager oversees regulatory labelling activities, manages associates, coordinates with stakeholders, and ensures compliance with guidelines and legislation.