Analytical Method Validation Chemist - Cuajimalpa

Description

Job Summary: Liomont Laboratories is seeking an Analytical Method Validation Chemist to develop and validate analytical methods, perform analyses, and participate in stability studies. Key Highlights: 1. Analytical method development and validation 2. Raw material and product analysis, participation in stability studies 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 • Flexible working hours Knowledge: • Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Documentation Practices • Pharmacopoeias and NOM-059 regulations • Analytical method validation according to national and international guidelines • Operation of equipment: 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 an updated CV.-Requirements- Minimum education: Higher education - Bachelor's degree 2 years of experience Languages: English Age: between 28 and 45 years