Job Summary: Perform documentation verification, product inspection, retention sample storage, and return management, ensuring compliance with GMP and GAP. Key Responsibilities: 1. Complete and compliant documentation verification. 2. Product inspection and retention sample storage. 3. Compliance with GMP and GAP for quality products. 1. Verify that product entry documentation is complete and compliant. 2. Conduct product inspection and retention sample storage together with the Assistant Pharmaceutical Chemist. 3. Inspect returned products and withdraw expired retention samples for destruction. 4. Record all performed activities in the respective forms. 5. Comply with GMP and GAP requirements to deliver quality products. 6. Carry out instructions provided by Technical Management and/or the Assistant Pharmaceutical Chemist of Technical Management. Employment Type: Full-time Application Question(s): * Are you available to work in the District of Lurín? * What is your salary expectation? * What is your academic degree? Work Location: On-site employment