**Job Function**: Quality **Job Sub**Function**: Customer/Commercial Quality **Job Category**: Professional **All Job Posting Locations**: Bogotá, Distrito Capital, Colombia We are searching for the best talent for Total Rewards Benefits Analyst to be based in Bogotá **The Commercial Quality Specialist will**: - Conducts Supplier & Distributor audits. - Manage the activities associated with the selection, qualification and approval of products or services suppliers/distributors that are within the scope of the quality management system, in accordance with current procedures. - Ensure the maintenance of suppliers and distributors requirements qualification. - Perform transactions in SAP for develop the master data process approval as DDL or GMP. - Support responses to address external audit and inspections. - Responsible for reporting, tracking and timely closure of audit (supplier, distributor & external) applicable corrective and preventive actions. - Management PQI and RC Alerts - Performs & reports compliance metrics and drive improvement on those metrics. - Management of technical assistance complaints, ensuring that actions plans are defined and communicated to customers as applicable. - Support the execution of the change controls, when applicable. - Support the execution of the complaint management process within the guidelines defined by the company - Execute the Post Market Surveillance processes: Technovigilance. - Execute local process for Compliance Alerts (FA, SS, Recall Etc..) ensuring that notifications are carried out and the affected product is handled in a timely manner, in line with current procedures. - Execute the CRAC (Regional coordinator of field actions) role when applicable. - Support the implementation of company standards such as: Temperature Control, Loaner Kits, Repack and Relabel, among others as applicable. - Support activities to execute the Management Review process. - Ensure compliance with Intercompany Quality Agreements Requirements. - Support the creation of the purchase orders relative to the process in the Commercial Quality area.Document Non-Conformities in the DES; ensuring compliance with the different stages: identification, investigation, cause analysis, correction, implementation of corrective and preventive actions and verification of effectiveness. **Qualifications**: - A minimum of 5 years of work experience in Quality Systems (Good Manufacturing Practices) is required. - Experience being a Lead Auditor - Title of pharmacist, life sciences, engineering, or other fields related to health sciences with expertise in Quality Systems. - English proficiency is required. - Proficiency in Microsoft Office is required. - Knowledge in SAP is desirable. - Strong analytical skills to identify areas for improvement in quality processes.