What your responsibilities will include:

• Organize coordinated efforts to ensure the proper functioning of the company's quality system in accordance with the requirements and principles of national and international requirements of pharmaceutical good practices (GMP and GDP) and ISO 9001 series standard.
• Organize the development, approval and submission for approval of quality system documentation, monitor their status, inform the staff in a timely manner.
• Maintain the proper functioning of the change control system for the quality system in the company.
• Supervise the validation work of technological processes, cleaning methods, analytical methods and systems/equipment qualification.
• Plan and conduct quality system self-inspections and prepare plant units to undergo external inspections

What is required of you:

• Higher education: pharmaceutical or chemical engineering
• At least 3 years of work experience in pharmaceutical production, QA or QC laboratory.
• Knowledge of Adobe pro, minitab, visio software
• Knowledge of information processing methods with application of modern technical means.
• Knowledge of the national and international normative-legal acts in the sphere of drug circulation.
• Knowledge of national and international requirements of pharmaceutical practices (GMP and GDP) and MS ISO 9001.
• Knowledge of the basics of production technologies.
• English - upper-intermediate (preferred), Russian, Kazakh.

We offer:

• Work schedule: 5/2;
• meals, shuttle service;
• annual bonus;
• Medical insurance (after the probationary period).