Job Description: * Bachelor’s degree completed or currently pursuing in Chemistry, Chemical Engineering, Biology, or Pharmacy (Mandatory); * SAP system knowledge preferred; * Total Productive Maintenance (TPM) knowledge preferred; * Quality culture knowledge preferred (5S, Good Laboratory Practices); * Data analysis knowledge preferred; * Microsoft Office Suite proficiency preferred. Note: Working hours are from 8:00 AM to 6:00 PM. * Manage non-conforming products; validate and release reprocessed products; create system-related hold entries for blocked items; manage the training matrix; * Identify training needs related to quality document reviews using the training matrix, and update the matrix according to completed trainings; * Manage suppliers and oversee Occurrence Reports (opening, validation); control inventory of blocked products; coordinate supplier visits and manage Quality Unavailability Follow-up Reports; * Execute quality-related processes/equipment/methods/analytical systems and perform necessary tests to compile validation reports; manage the training matrix; monitor document revisions in the document management software (SYD); * Ensure analytical methodology and metrological reliability; support execution of analyses and inspections per published standards; maintain inventory of critical equipment; * Manage equipment calibration and equipment sent for maintenance; deliver metrological reliability training to personnel with identified gaps; manage routing of critical equipment; * Manage non-conforming products and conduct physical vs. system inventory reconciliations; support operator training on quality concepts; * Understand and apply practices of conscious consumption and natural resource preservation in compliance with the company’s SSMA policies, recognizing environmental impacts and risks, and familiarizing oneself with emergency response procedures. 2512090203141855186