Analista del controllo qualità

NerPharMa operates as a CDMO (Contract Development and Manufacturing Organization) and offers unparalleled expertise in bringing highly potent compounds to the marketplace. NerPharMa has brought new products and unique innovative technologies to the market over the years, delivering a wide range of GMP services through its agile and flexible facilities. NerPharMa owns a wide and cutting-edge organizational structure able to manage and handle highly active compounds, and to ensure the full development and production of active principles and finished products intended for the world market as well as the research and development of innovative formulation and delivery systems. About the position: QC Chemical Analyst We are looking for a young graduate to join Nerpharma’s Quality Control Department, specifically in the chemical team that is responsible for Drug Product analytical management (release, stability, and validations). Key Responsibilities: Application of general analytical techniques, specifically chromatographic methods, spectrophotometry, potentiometry, and chemical-physical methods in accordance with pharmacopoeias and in-house methods. Performing the analyses required for the manufacture and control of drug products, intermediates, and excipients, analysis of stability samples, and validation of analytical methods. Use of IT tools to support analytical activities, including specific tools (i.e., LIMS) for collecting and archiving analytical data. Manage analytical documentation (issue, revision). Carrying out assigned activities in accordance with cGMP and in compliance with safety regulations. Use of analytical instrumentation according to cGMP requirements. Care of the assigned instrumentation to maintain it at the highest level of efficiency through periodic maintenance, calibration, and qualification. Qualifications & Experience: Minimum required Bachelor Degree in Chemistry, CTF, or a related scientific field. Experience in analytical laboratories, preferably with experience in the use of GC and HPLC managed by Empower. Knowledge of GMP. Knowledge of main Microsoft Office packages. Attitude for problem-solving, proactivity, and teamwork. Good knowledge of written and spoken English. Seniority level Entry level Employment type Full-time Job function Analyst, Quality Assurance, and Production Pharmaceutical Manufacturing J-18808-Ljbffr

Location: nerviano, IT

Posted Date: 1/23/2025