Job Mission Ensure the quality, safety, and technical compliance of compounded medications by working directly in the laboratory, supervising auxiliary staff, and guaranteeing adherence to Good Compounding Practices, health regulations, and current legislation. Key Responsibilities Supervise and monitor **all stages of the medication compounding process**, from weighing to final product release. Guide, train, and supervise the **laboratory auxiliary staff team**, ensuring standardization, organization, and technical quality. Guarantee compliance with **Good Compounding Practices (GCP)** and regulations issued by **ANVISA**, the Regional Council of Pharmacy (CRF), and health surveillance authorities. Verify formulas, prescriptions, and compounding orders, assessing **technical feasibility and pharmaceutical compatibility**. Monitor and validate **Standard Operating Procedures (SOPs)** and laboratory records. Control and supervise the use of **raw materials, supplies, and equipment**, ensuring appropriate storage and traceability. Act as the **technical responsible person**, where applicable, maintaining updated documentation, licenses, and records. Requirements Bachelor’s degree in **Pharmacy**, with an **active CRF registration**. Experience in **compounding/handcrafted pharmacy**. Knowledge of **Good Compounding Practices** and current health legislation. Experience in **supervising laboratory teams** will be considered a plus.