Job description

• Supervision over the process of preparing and conducting internal audits / external audits. Assessing the functioning of the quality system in the audited units.
• Supervision over the process of preparing and conducting qualification for manufacturers/ suppliers/ service.
• Supervision over the process of preparing and conducting of the Quality Agreements with manufacturers/ suppliers/ service.
• Performing internal trainings (as a trainer) of procedures/ instructions/ amendments system to quality documents and guidelines of the Pharmaceutical Quality System.
• Implementation of system activities in accordance with the guidelines and quality risk management.
• Organization, implementation and improvement of the Pharmaceutical Quality System. Controls and assessment of the functioning of the quality system in Davipharm.
• Participation in the corrective and preventive actions (CAPA) to ensure the effective and timely implementation in accordance with the implemented procedure, including initiation of actions to prevent non-compliance.
• Establishing indicators for the improvement of quality processes and ensuring their implementation.
• Implementation of designated projects for the development of the Pharmaceutical Quality System in Davipharm.
• Participation in the investigation of complaints, ensuring their efficient and timely implementation in accordance with the implemented procedure. Assessment of the impact of the complaint on the product on the market.
• Coordination of activities leading to compliance with Pharmaceutical law and GMP requirements.
• Supporting the operational activities related to the availability of Davipharm products in accordance with the objectives.Certification and releasing product to the market.
• Team management in terms of achieving business goals, team development, prioritizing, recruiting.
• Coordination of activities in all departments before and during external audit and inspections in Davipharm.
• Do other ad-hoc assignments from direct supervisor.

Job requirement

• Bachelor of Pharmacist.
• At least 3 years of experience in similar role.
• Knowledge of pharmaceutical law, GMP requirements, manufacturing processes, testing processes, validation
• Excellent knowledge of the implementation of Pharmaceutical Quality system.
• At least 2 years of experience in pharmaceutical factory.
• Ability to analyze and solve problems.
• Ability to work under high pressure and intensive deadlines.
• Understand the systematic process of WHO GMP, EU GMP in the pharmaceutical industry.
• MS Office 365: Microsoft Excel, Word, PowerPoint.
• Ability to interact with colleagues at all levels throughout the company.
• Support other departments at work.
• Good command of English skills.

Please contact our Recruiter or apply via email recruitment@davipharm.info