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Technical Director Assistant / Work in Comas

S/1,800-2,000/month
Indeed

Company

Job typeFull-time
Workplace typeOnsite
Experience levelNo experience limit
Education levelNo degree limit

Description

Job Summary: TECHNICAL DIRECTOR ASSISTANT responsible for monitoring pharmaceutical product storage and distribution in accordance with health regulations. Key Responsibilities: 1. Monitor pharmaceutical product storage and distribution. 2. Ensure compliance with the Quality Management System. 3. Control observed, rejected, expired, etc. products. **LAFARMED** A company dedicated to the marketing of pharmaceutical products throughout Peru. The quality of our products and services has enabled us to achieve solid growth in the pharmaceutical market share. We invite you to join our team in the position of **TECHNICAL DIRECTOR ASSISTANT** **RESPONSIBILITIES**: \- Ensure that pharmaceutical product storage and distribution comply with current health regulations and applicable Good Practices. \- Maintain and ensure compliance with the company's implemented Quality Management System, as applicable. \- Supervise product receipt, storage, preservation, distribution, and transportation conditions. \- Verify that marketed products possess valid health documentation and meet applicable regulatory requirements. \- Control and supervise observed, rejected, expired, deteriorated, returned, or market-recalled products. \- Keep technical documentation up to date. \- Participate in pharmacovigilance activities and in managing adverse incidents related to medical devices. \- Maintain technical and health records required by current regulations. \- Promptly inform the Technical Director of any situation that may affect product quality, safety, or performance. **REQUIREMENTS**: . \- Professional degree in Pharmaceutical Chemistry. \- Valid professional license and registration. \- One year of experience in this position. \- Accredited training in Good Storage Practices (GSP) and applicable health regulations (preferred). \- Knowledge of regulatory affairs in Quality Management Systems, Regulatory Affairs, Pharmacovigilance, or Risk Management (preferred). \- Proven experience in pharmaceutical establishments (pharmacies, laboratories, \- Experience in evaluating and managing risks related to product quality, safety, and performance. **BENEFITS**: SALARY ON PAYROLL with 100% statutory benefits (CTS, bonuses, profit-sharing, vacation, EsSalud, etc.). \- WORK HOURS: Mon-Fri: 8:00am-5:30pm / Sat: 8:00am-1:30pm Employment Type: Full-time Work Location: On-site employment Send your CV to Phone: 922231070 Salary: S/.1,800\.00 - S/.2,000\.00 per month Work Location: On-site employment

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Posted by

María García

Indeed · HR

Location

María García

Indeed · HR

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