Production Director

Ensuring the planning and organization of production and storage of medicinal products in accordance with the requirements of state regulatory authorities and GMP; Leading technological transfers, process validation, and equipment qualification, approving regulations and SOPs; Preparing production for inspections and external audits, managing deviations and changes (Change Control); Modernization of capacities, implementation of new drugs, automation, and optimization of production processes.

Requirements

Higher professional education (chemical-technological/pharmaceutical/biotechnological), professional development every 5 years; Management experience in solid dosage form production for 7+ years, mandatory in international companies; Experience in production and personnel planning, technological transfers, process optimization and validation, and preparation for inspections; Knowledge of GMP EU and Russia, licensing requirements, validation principles, equipment qualification, risk management, and statistical quality control methods; Project management skills, supplier assessment, URS development, automation, and negotiation skills; English language at least B2, analytical thinking, stress resistance, multitasking, result orientation.

Higher education — specialist degree, master's degree; Experience: 6 years