P Position: Pharmacometrician Scientist /pp Location: Azuqueca de Henares. /pp Experience: 2 to 4 years in similar roles. /p pb Do you want to know more? /b /p p INSUD PHARMA operates throughout the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to both human and animal health. /pp INSUD PHARMA’s activity is structured into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with more than 9,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialized RD centers, 12 commercial offices, and over 35 pharmaceutical subsidiaries, serving 1,150 clients in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. /pp Are you ready to be a #Challenger? /pp What are we looking for? /p pb The challenge! /b /p ulli Provide technical and scientific support for NME and complex generic development projects, driving appropriate biopharmaceutical assessment and contributing to the selection of formulation prototypes. /lili Identify relationships between drug substance properties, dosage forms, drug release, and drug absorption. /lili Build mathematical models describing formulation effects on drug absorption (IVIVC and PBPK models). /lili Develop predictive PK models based on in vitro dissolution data (IVIVC). /lili In collaboration with other team members, develop PK/PD models to address questions related to complex generic products. /lili Contribute to the implementation of new tools and solutions to strengthen in vitro–in vivo relationships within the department. /lili Author, review, and contribute to scientific documentation and technical reports to support regulatory submissions (including scientific advice packages and responses to deficiency letters). /lili Interact and collaborate scientifically with internal cross-functional project teams and external partners. /lili Maintain compliance with internal SOPs, regulatory guidelines (ICH, EMA, FDA), and GCP/GLP quality standards. /li /ul pb What do you need? /b /p ulli University degree in Pharmacy, Bioinformatics, Biopharmaceutics, or other related sciences. /lili PhD in data modeling or related field is a plus. /lili Strong background in pharmacokinetics and IVIVC. /lili Knowledge of in vitro dissolution testing (biorelevant/biopredictive API and formulation testing). /lili Hands-on experience with programming languages such as R or Python. /lili Experience with pharmacometric and PBPK platforms such as Phoenix, NONMEM, Simcyp, GastroPlus, PK-Sim, or equivalent tools. /lili High level of English (spoken and written). /lili Intermediate level of Spanish. /li /ul pb Our benefits! /b /p p⏰Flexible entry schedule from Monday to Friday (full-time, 40 hours). /pp Permanent contract /pp Attractive salary package. /p