Position Summary: Liomont Laboratories is seeking an Analytical Method Validation Chemist to develop and validate analytical methods and perform physicochemical analyses, ensuring regulatory compliance. Key Highlights: 1. Experience in analytical method development and validation 2. Proficiency with equipment such as HPLC, UPLC, and gas chromatography 3. Opportunity for professional growth Liomont Laboratories is seeking Analytical Method Validation Chemist Requirements: • Education: Bachelor’s degree in Pharmacy and Biochemistry (Q.F.B.), Industrial Pharmacy (Q.F.I.), Chemistry, or Chemical Engineering • Experience: 2 years in analytical method development and/or validation • Availability to work flexible hours Knowledge: • Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Documentation Practices • Pharmacopoeias and NOM-059 regulations • Analytical method validation in accordance with national and international guidelines • Equipment operation: HPLC, UPLC (Waters) • Empower 3.0 / 3.0.8 software • Gas chromatography • Physicochemical analysis Main Responsibilities: • Development and validation of analytical methods for raw materials and cleaning processes • Analysis of raw materials, finished products, and dissolution profiles • Execution of tests for product development or reformulation • Participation in stability studies and process validation • Adherence to timelines and applicable regulations We Offer: • Competitive salary • Statutory benefits • Job stability • Opportunity for professional growth Work Location: CDMX - Cuajimalpa Working Hours: Monday to Friday 7:00 a.m. to 4:00 p.m. Interested Candidates: Apply through this channel if you fully meet the profile, or send your updated CV.-Requirements- Minimum education: Higher education - Bachelor’s degree 2 years of experience Languages: English Age: between 28 and 45 years