**Functions:** 1\. Support the preparation of documentation related to pre-settlement, certification requests, and management of supporting documents for BPM. 2\. Follow up on files at the Ministry of Health, including modifications, extensions, changes, reimbursement of travel allowances, and updating of certifications to ensure continuous marketing of products and expand the company’s product portfolio. 3\. Participate in inspections of the integrated management system and comply with Good Manufacturing Practices, Good Storage Practices, and Good Distribution and Transportation Practices to ensure the preservation, stability, and quality of pharmaceutical products, medical devices, and sanitary products. 4\. Review technical documents from production, quality control, and quality assurance departments for contract manufacturing. 5\. Review and maintain the pharmacy’s technical documentation, keeping current archives of files and procedures within the department. 6\. Support inspections to verify facility maintenance and comply with instructions provided by the Technical Management Department and/or the Assistant Pharmaceutical Chemist of the Technical Management Department. 7\. Carry out proper storage of the retention sample for each batch. 8\. Support the review of returns and withdrawal of expired retention samples for destruction. 9\. Other duties assigned by the immediate supervisor. **Benefits:** \-FOLA Health Insurance \-Fixed working hours Monday through Friday, 7:00 a.m. to 5:00 p.m. \-Bi-weekly and end-of-month payments. \-Additional bonus equivalent to half a month’s salary for every six months of internship. **Requirements:** \-Graduate or bachelor’s degree holder in Pharmacy and Biochemistry. Employment type: Full-time Application question(s): * Are you a graduate or bachelor’s degree holder in Pharmacy and Biochemistry? * Are you available to work in Lurín? * What are your salary expectations? Work location: On-site employment