Analytical Development MS Analyst /Specialist

Founded in 1912, Abdi İbrahim has the broadest product portfolio in the pharmaceutical industry and employs 5,500 qualified professionals, creating the highest level of employment in the Turkish pharmaceutical sector. With a strong vision, Abdi İbrahim has maintained its leadership in the Turkish pharmaceutical market since 2002.

Today, Abdi İbrahim operates in 17 countries outside of Turkey and exports to more than 70 countries across a wide geography—from Canada to EU member states, and from North Africa to Asia and the Middle East. With its corporate citizenship identity, sectoral mission, and social priorities, Abdi İbrahim works toward a better world and a better future, maintaining a sustainability-focused approach across all business processes.

In line with its 2030 vision , Abdi İbrahim continues to strengthen its international presence while maintaining its strong national leadership, aiming to rank among the world’s top 100 pharmaceutical companies .

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

Qualifications

• Bachelor’s degree in Chemistry or Chemical Engineering
• Preferably a Master’s or PhD degree in Organic Chemistry, Analytical Chemistry, or Pharmaceutical Chemistry
• Minimum 2 years of analytical experience in qualitative and quantitative analysis using MS instruments (LC-MS, GC-MS) is required for the specialist role,
• Knowledge of analytical method development, method validation, genotoxic impurities, nitrosamine analyses, extractable & leachable analyses, and impurity structure elucidation
• Excellent command of written and spoken English (capable of following current publications and regulatory guidelines)
• Strong analytical and problem-solving skills
• Team-oriented with effective communication skills

Job Description

• Develop and validate analytical methods for Genotoxic Impurities and Nitrosamine Impurities in finished products, in compliance with regulatory requirements, and prepare validation reports
• Perform and interpret Genotoxic Impurity and Nitrosamine Impurity analyses in raw materials and finished products during new product development
• Develop and validate analytical methods for Extractable & Leachable impurities in compliance with regulatory standards, and prepare related reports
• Conduct and interpret Extractable & Leachable impurity analyses in finished products during new product development
• Perform impurity identification and characterization studies for unknown impurities formed during new product development