
Quality Manager CIS/Responsible Person Kazakhstan
- Алматы
- Постоянная работа
- Полная занятость
- Act as Qualified Person for Kazakhstan, overseeing batch release, documentation, sampling, inspections, and final disposition of products.
- Implement and maintain a robust Quality Management System (QMS) at LOC level for all marketed products.
- Manage operational quality activities including batch management, repacking, recalls, complaints, and logistics oversight.
- Ensure timely escalation and resolution of quality incidents.
- Provide oversight on GxP-related third-party activities.
- Participate in LOC Quality Council and local RMCB, escalating risks as needed.
- Collaborate with supply chain and CS&L teams to ensure quality excellence across operations.
- Degree in Pharmacy.
- Valid certificate as Responsible Person in Kazakhstan (per Ministry of Health regulations: ҚР ДСМ-148/2020, ҚР ДСМ-274/2020, ҚР ДСМ-249/2020).
- Minimum 3–5 years of experience in Pharmaceutical or Consumer Healthcare Quality Assurance, Compliance, or Quality Control.
- At least 1 year of GDP QA experience.
- Strong knowledge of GMP/GDP and regulatory requirements.
- Experience with LOC Quality activities (e.g., batch release, product incidents, third-party management).
- Excellent oral and written communication skills.
- Fluent in English.
- Strong interpersonal, negotiation, and problem-solving skills.
- Proven ability to influence across business levels and drive change.
- Self-starter with the ability to manage workload independently.
- Experience working with CIS markets.
- Familiarity with inspection readiness and complaint management processes.
- Knowledge of effective quality documentation systems.
- Performance-based bonuses.
- Corporate Health Insurance Scheme.
- Travel Insurance.
- Meal allowance.
- Mobile phone and laptop.
- Sport compensation.
- Employee Assistance Programme.