Responsibilities:

• Lead the quality department (quality control and quality assurance).
• Act as the Authorized Person in the company: confirm compliance of each series of medicinal product with the established requirements and authorize sales to the domestic pharmaceutical market or for export.
• Maintain the operation of the company's basic quality standards.
• Develop, coordinate and approve quality assurance and quality control documentation.
• Requirements:
• Higher pharmaceutical, medical (basic and clinical medicine), biological or chemical education,
• 5 years working experience in the field
• Knowledge of legislation of the Russian Federation in the field of production and quality control of medicines and international rules of the organization of production and quality control of medicines (GMP & GLP);
• Knowledge of the technology of solid dosage forms production and methods of drug control, modern requirements for the organization of quality control laboratories activities in relation to the tasks assigned to the quality service.

Conditions:

• Registration under the Labor Code of the Russian Federation
• Work schedule: 5 / 2.
• Place of work - Kazan (rent is at the expense of the company)