QAC Specialist - BRR

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: Ensure compliance and completeness of the Batch Record, through collection and analysis of all necessary documentation; Documentary verification of material approval status, of check list and current SOPs, in compliance with applicable regulations (laws, GMP regulations, FDA, etc.) and company quality standards. Requisiti: MA degree (CTF/Chemistry) English working knowledge Great can-do attitude Altre informazioni: 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. J-18808-Ljbffr

Location: provincia-di-latina, IT

Posted Date: 2/22/2025