Job Summary: TECNALIA seeks a proactive and responsible individual to develop innovative pharmaceutical formulations for new medications, contributing to applied research and technology transfer. Key Highlights: 1. Professional development opportunities. 2. Integration into a young and dynamic team. 3. Work-life balance measures. TECNALIA has the experience and infrastructure required to carry out the formulation development of a wide range of products. We operate the only national platform covering the entire drug development process—from formulation, analytical validation, and pilot batch manufacturing to clinical trials. TECNALIA’s Pharmaceutical Development Laboratory holds accreditation from the Spanish Agency of Medicines and Medical Devices (AEMPS) for Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). We aim to strengthen this Pharmaceutical Development Laboratory and, to that end, seek to hire a professional dedicated to developing new drugs based on innovative galenic formulations. *If you are proactive, responsible, solution-oriented, adaptable to new projects, and enjoy teamwork…* *If you are interested in applied research and in transferring technology to companies and society to address future challenges… keep reading…!* ***Your Responsibilities:*** * Proposing galenic formulations and evaluating their physicochemical characterization and in vitro studies. * Developing and validating analytical methods. * Conducting stability studies on selected prototypes. * Preparing associated documentation: technical reports, protocols, summaries, etc. * Managing proposals, planning, coordinating, and executing pharmaceutical development projects, adhering to principles of efficiency, profitability, and customer satisfaction. ***What We Offer:*** * *Professional development opportunities.* * *Integration into a young and dynamic team.* * *Work-life balance measures.* * *Permanent contract.* **Qualifications:** Bachelor’s degree in Pharmacy or Health Sciences **Languages:** Proficiency in English—reading, comprehension, and fluent conversation. Minimum level B2 **Experience:** 2 years in a similar position **Desirable Qualifications:** * Knowledge of Good Manufacturing Practices (GMP) for medicinal products. * Knowledge of Good Laboratory Practices (GLP). * Laboratory experience and familiarity with physicochemical techniques. * Chromatographic expertise (HPLC) and proficiency with analytical software (e.g., EMPOWER, OpenLab…). * Experience in similar roles. * Master’s degree in the pharmaceutical industry. * *We positively consider applications from individuals holding a disability certificate of 33% or higher, in compliance with current legislation—the General Law on the Rights of Persons with Disabilities and Social Inclusion (LGD).*