QA Validation Specialist

BSP Pharmaceuticals S.p.A is a Contract Development and Manufacturing Organization (CDMO). The BSP campus hosts 2 segregated facilities to serve the clients with development from pre-clinical GLP to cGMP manufacturing for clinical and commercial supply of Cytotoxic and High Potent Oncology drugs and Non-Cytotoxic, innovative compounds for Immunotherapy and other therapeutics applications. Facilities designed to handle small and large molecules as ADCs (conjugation and fill finish), Peptides, Proteins, Oligonucleotides and Nano Medicines. BSP is technologically developed to meet the needs of innovators, with its High Containment Facility designed to offer a full range of integrated services aimed to support the entire life cycle of a product, from the formulation and process development/optimization, through scale up/scale down studies. Posizione: We are currently looking for a QA Validation Specialist for our Quality Assurance Validation Team. Main Activities: Analysis of technical documentation: Ensure the analysis and evaluation of technical documentation related to manufacturing processes or cleaning and sanitization procedures that have to be submitted for validation. Defining Protocols: Drafting the Validation Protocols, by researching and acquiring data and information from other business functions. Validation: Ensure the correct validation of the processes, cleaning in compliance with company protocols and procedures through the execution of the operational activities. Preparation of Validation Reports. Data Analysis: Ensure correct analysis of validation activities through data collection and analysis, in compliance with company protocols and procedures. Main Requirements: MA degree (CTF/Chemistry) 1/2 years of experience in similar roles in complex organizations Knowledge of GMP English working knowledge Great can-do attitude At BSP we believe in an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. We respect diversity, the different backgrounds and experiences and provide equal opportunity for all. We are BSP. Seniority level Entry level Employment type Full-time Job function Quality Assurance Pharmaceutical Manufacturing J-18808-Ljbffr

Location: provincia-di-latina, IT

Posted Date: 4/12/2025