R&D Analytical Development Analyst/Specialist

Abdi İbrahim, founded in 1912, has the largest product portfolio in the sector and is the largest employer in the Turkish pharmaceutical industry with 5.500 employees. Abdi İbrahim has been the leader of Turkey’s pharmaceutical industry since 2002 with its powerful vision.

Today, Abdi İbrahim operates in 17 countries outside Türkiye, exports to more than 70 countries ranging from Canada to European Union member states, from North Africa to Asia. As a corporate citizen working towards creating a better world and a better future, adhering to its mission in the sector and to the requirements of societal priorities, Abdi İbrahim focuses on sustainability in all its business processes.

Its vision for 2025 - apart from maintaining its status as a wholly local company - is to become "one of the top 100 pharmaceutical companies in the world.

We are looking for an " Analytical Development Analyst/Specialist " to join our R&D Center located in Esenyurt.

Qualifications

• Graduated from Chemistry or Chemical Engineering departments,
• Preferably holding or currently pursuing a Master’s degree in Analytical Chemistry or Pharmaceutical Chemistry,
• Minimum 2 years of analytical experience is required for the specialist role,
• Excellent command of English (both written and verbal),
• Strong teamwork and communication skills,
• Knowledge and hands-on experience in analytical method development, method validation, and stability studies,
• Ability to follow up-to-date scientific publications and regulatory guidelines in English,
• Analytical thinker with strong problem-solving orientation.

Job Description

• Conduct literature research for raw materials and finished products related to newly approved product development projects,
• Perform analytical method development, validation, and required testing activities, and prepare corresponding reports in compliance with applicable requirements,
• Carry out stability analyses for new products, prepare and evaluate stability reports in line with regulations,
• Prepare analytical documentation sections of registration dossiers in CTD format for submission to the Ministry of Health.