Technical Director Assistant - Pharmaceutical Laboratory

Description

Job Summary: We are seeking a Technical Director Assistant responsible for managing and ensuring the updating, control, and custody of manufacturing records and technical documentation. Key Responsibilities: 1. Manages and ensures the updating of records and technical documentation. 2. Prepares and manages regulatory procedures before DIGEMID. 3. Ensures compliance with regulations regarding product destruction. Join our team and contribute to improving people's health and quality of life! At Elifarma, we are looking for a **Technical Director Assistant**, responsible for managing and ensuring the updating, control, and custody of manufacturing records, master formulas, and the company's technical documentation. **Requirements:** * Bachelor's degree in Pharmacy and Biochemistry. * Knowledge of GMP, GLP, or GCP (desirable). * Proficient user-level knowledge of Microsoft Office. * Intermediate-level English proficiency. * Availability to work on-site in Ate, Monday through Friday, from 7:00 a.m. to 4:30 p.m. **Responsibilities:** * Conducts, in coordination with the Technical Director, mock drills and market withdrawal processes as required, preparing the necessary technical documentation and reports. * Issues, reviews, controls, and maintains custody of manufacturing records and master formulas for company products, ensuring their timely updates in systems and compliance with established procedures. * Prepares, manages, and follows up on regulatory procedures before DIGEMID related to controlled substances, sanitary registrations, modifications, re-registrations, technical consultations, and other applicable regulatory requirements. * Maintains updated regulatory documentation and records associated with controlled substances, guaranteeing compliance with provisions issued by competent authorities. * Manages product destruction processes for expired, deteriorated, contaminated, rejected, or withdrawn products, ensuring compliance with current regulations and preventing accumulation. * Prepares and submits regulatory information required by health authorities, including periodic price declarations and other mandatory reports. * Manages the control and updating of product labels, ensuring implementation of approved changes within the Quality Management System. * Registers, monitors, and reports area performance indicators, as well as coordinates execution of customer satisfaction surveys and consolidation of their results. **Benefits:** * Half-day off on your birthday. * Corporate agreements with Soho, Sise, Senati, Valora, etc. * Continuous learning and departmental mentoring. * Positive work environment and collaborative culture. * 70% food subsidy Salary: S/.1\.00 \- S/.2\.00 per month Application Question(s): * Do you have experience in this position? Please detail. * Do you have knowledge of GMP, GLP, or GCP? With or without certification? Please detail. * Are you available to work overtime? * Please share your salary expectations. Work Location: On-site employment