Description: To participate in our process: * Bachelor’s degree completed or in progress in Chemistry or Pharmacy; * Experience in a quality control or stability laboratory within the pharmaceutical sector; * Solid experience in benchtop analysis. You will stand out if you have: * Mandatory knowledge of HPLC and GC. On a day-to-day basis, you will: Perform quality analyses on finished products, analyzing results and verifying whether they comply with specifications; Analyze existing methods, evaluating whether the process is being carried out according to established procedures, with the aim of proposing improvements; Prepare reports with the results obtained from analytical validation studies of new analytical methods; Execute the implementation protocol for new analytical methods originating from other units, evaluating whether the results comply; Develop new analytical methods for cleaning monitoring and for in-process control of finished products; Investigate non-conformities identified in quality assurance systems, as well as prepare protocols and procedures for correcting and preventing such quality errors; Ensure proper maintenance of equipment and instruments used, as well as organization and cleanliness of the laboratory facilities. 2512180202551924978