**At Psicofarma, a Mexican pharmaceutical company with over 45 years of commitment to health and quality, we continue growing and strengthening our operations.** **Location:** Toluca **Work Mode:** On-site **Schedule:** Full-time ### **Responsibilities:** * Perform analytical method validation for raw materials and finished products * Develop or update departmental procedures. * Draft validation protocols and reports in accordance with current regulations (FDA, ICH, NOMs) * Work with instrumental techniques such as HPLC, UV, IR, dissolution, among others * Collaborate with Development, Quality, and Production departments to ensure method robustness * Comply with Good Laboratory Practices and documentation (GLP, GMP) ### **Profile We Are Seeking:** * Bachelor’s degree in Pharmacy & Biochemistry (QFB), Chemical Engineering (IQ), Food Chemistry (QFI), or related field * Minimum 2 years of experience in analytical method validation and transfer within the pharmaceutical industry * Knowledge of USP Pharmacopeia, NOMs, and ICH Q2 guidelines * Proficiency in analytical equipment and software (Empower, OpenLab or similar) * Analytical skills, results-oriented mindset, and teamwork ability ### **We Offer:** * Direct employment with Psicofarma * Benefits exceeding legal requirements * Savings fund * Grocery vouchers * Subsidized cafeteria * Parking * Professional stability and development within the pharmaceutical industry