About the client

We are working with a leading European specialty pharmaceutical company focused on the treatment of central nervous system (CNS) disorders that is currently seeking an Analytical Development Senior Scientist. Mission

Design, develop, organize, perform, review, evaluate and report any analytical test according to the established quad guidelines (GxP, ICH, etc.) and the corresponding SOP to ensure reliability and quality data for the registration and marketing of new pharmaceutical drug products. Major Accountabilities

Distribute, review, analyze and report all results of assigned projects to meet deadlines (development studies, validations, stability studies, etc.) in agreement with the project team. Develop, verify and/or validate required analytical methods. Work effectively and independently, adapting to a fast‑paced, rapidly changing environment, reporting to the team leader.





Write and/or review SOPs and other relevant documents as part of analytical validation reports. Write different sections of Module III of the registration dossier in collaboration with Galenical scientists. Ensure correct calibration and maintenance of assigned instruments and equipment.

Represent the Analysis Section in assigned project team meetings. Qualifications

At least 3 years of experience developing similar functions in the pharmaceutical industry and working to EU GMP standards. Educational background in analytical techniques (HPLC, GC, ICP, MS, IFL, etc.). Proficiency with user‑level computer tools. Knowledge of risk assessment. Degree in chemical or pharmaceutical sciences. Proficiency in Spanish and English (minimum B2). Organized, planned, and strong team spirit.

📌 Analytical Development Senior Scientist (Madrid)
🏢 Actual Talent
📍 Madrid