Hello. We’re Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we’re improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands – including Sensodyne, Panadol, Advil, Voltaren, parodontax, Otrivin, and Centrum – through a unique combination of deep human understanding and trusted science. What’s more, we’re achieving it in a company that we’re in control of. In an environment that we’re co-creating. And a culture that’s uniquely ours. Care to join us. It isn’t a question.

This is an exciting time to join us and help shape the future. It’s an opportunity to be part of something special.

About the role:

We are seeking a dedicated Quality Representative / Responsible Person for the Kazakhstan market, who will also support quality operations across CIS countries including Belarus, Kyrgyzstan, Tajikistan, Uzbekistan, Azerbaijan, Armenia, Georgia, Turkmenistan, Mongolia, and Kazakhstan. This role ensures compliance with GMP/GDP and local regulatory requirements, and acts as the key quality contact for local authorities and the Export Market Quality Lead.

Your Day to Day:

• 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.

Ideal Candidate Profile:

• 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.

Preferred:

• Experience working with CIS markets.
• Familiarity with inspection readiness and complaint management processes.
• Knowledge of effective quality documentation systems.

Our Offer:

• Comprehensive Health Insurance.
• Life Insurance.
• Meal Allowance.
• Corporate car to make your commute comfortable.
• Mobile Benefit.
• Additional Vacation Days & Additional Vacation Pay.
• Additional Maternity and Paternity Leave.
• Fitness Compensation.
• Flexible Working Hours.
• Referral Program.
• Employee Assistance Programme (EAP).
• Travel and Expenses.