HPLC Quality Control Analyst

Description

Job Summary: We are seeking a proactive and rigorous Instrumental Quality Control Analyst to develop and optimize physicochemical analytical methods using instrumental techniques. Key Highlights: 1. Committed to animal health and high quality standards. 2. Development and optimization of analytical methods. 3. Guarantee of data integrity and compliance with GMP. **Who Are We?** At **LABET SAC**, we are a veterinary chemical laboratory committed to ensuring animal health through the highest quality standards. We are currently seeking a passionate, proactive, and highly technically rigorous **Instrumental Quality Control Analyst** to join our team. **Job Objective:** To execute, develop, validate, and optimize physicochemical analytical methods using instrumental techniques (HPLC, UV\-Vis, NIR), ensuring result integrity in compliance with Good Manufacturing Practices (GMP) and applicable regulations. **What Profile Are We Looking For?** * **Education:** Technician in chemical analysis, quality, industrial, food, chemistry, or related fields; or Bachelor's degree/Graduate in Pharmaceutical Chemistry, Chemistry, or Chemical Engineering. (CERTIFIED experience in instrumental analysis or analytical development is MANDATORY.) * **Experience:** Minimum 2 years in instrumental quality control laboratories, with **proven experience in HPLC operation** and in analytical method development/validation. **Required Technical Knowledge (MANDATORY):** * **Advanced-level liquid chromatography (HPLC).** * UV\-Vis spectrophotometry and NIR spectroscopy. * **Analytical method development and validation (ICH Q2\).** * Management of out-of-specification (OOS/OOT) results and data integrity (ALCOA\+). * Good Manufacturing Practices (GMP) regulations. **Key Competencies:** * **Proactivity and dynamism:** Ability to anticipate departmental needs, propose improvements to existing methods, and independently resolve problems. * High technical rigor, critical thinking, and professional ethics. * Ability to work autonomously and excellent documentation organization skills. **Main Responsibilities:** * Perform instrumental analyses of raw materials, in-process products, and finished products using HPLC, UV\-Vis, and NIR. * Develop and optimize analytical methods for quantification and identification of active pharmaceutical ingredients. * Execute validation, revalidation, and method transfer protocols according to international guidelines (ICH, pharmacopoeias). * Ensure data integrity under ALCOA\+ principles and maintain traceable data records. * Actively participate in the investigation and handling of deviations or out-of-specification (OOS/OOT) results. * Monitor, qualify (IQ, OQ, PQ), and coordinate maintenance of instrumental equipment in the department. **What Do We Offer?** * **Base salary:** PEN 3,000\.00 to PEN 3,500\.00 per month, subject to certified experience. * **Immediate payroll enrollment:** With statutory benefits (bonuses, CTS, vacation, ESSALUD as per law). * **Stability:** Direct employment contract with the company. **Fixed Working Hours:** * Monday to Friday: 8:00 a.m. to 5:00 p.m. * Saturdays: 8:00 a.m. to 12:00 p.m. Salary: PEN 3,000\.00 \- PEN 3,500\.00 per month Workplace: On-site employment