Quality Control Department

Roles & Responsibilities:
• Handle stability samples, manage stability chambers, and monitor stability data
• Prepare stability protocols, reports, trackers, and RM/IP/FP/hold time documents
• Conduct stability analysis using HPLC and UV techniques
• Operate, calibrate, and maintain HPLC instruments
• Perform assay, dissolution, related substances (RS), UOC, and swab/rinse analyses
• Conduct RM, IP, and FP analysis following IP/BP/USP/Ph.Eur. standards, with preference for OSD background in dissolution and calibration tasks
• Calibrate QC instruments including pH meters, balances, and other equipment
• Perform water testing, reagent and solution preparation, and manage chemicals and glassware
• Ensure compliance with GLP practices and maintain high-quality laboratory standards

Qualification:
• M.Sc, B.Pharm, or M.Pharm in Pharmacy, Chemistry, or related discipline

Experience:
• 1–4 years of experience in pharmaceutical quality control, preferably in oral solid dosage (OSD) formulations
• Hands-on experience with HPLC, stability studies, and GLP compliance

Skills:
• Strong knowledge of HPLC operation, stability studies, GLP practices, and pharmacopoeial standards (IP/BP/USP/Ph.Eur.)
• Attention to detail, analytical and problem-solving skills
• Ability to work in a regulated pharmaceutical environment
• Immediate joiners preferred

About the Organization:
Leben Life Sciences Pvt. Ltd. is a leading pharmaceutical formulation company with a state-of-the-art, EU-GMP compliant manufacturing facility in Akola, Maharashtra. The company is known for its focus on quality, innovation, and adherence to international regulatory standards. It provides professionals with the opportunity to work in a dynamic, high-quality environment, contributing to the development and assurance of safe and effective medicines.