Descrizione azienda 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 QC Chemical Analyst that will mainly ensure:
Chemical analysis of raw materials, semi-finished and finished products according to current analytical methods or Pharmacopoeias; Daily use and control of the main laboratory equipment (HPLC, UPLC, UV, SoloVPE, KF, IR); Manage capillary electrophoresis; Evaluation of analytical results obtained; Drafting of GMP documentation; Proper handling and use of reagents and laboratory standards; Use of major data processing and management software (Empower, Totalchrom, UV WinLab ES, Excel, LIMS). Requisiti MA degree (CTF/Chemistry...) At least 2 years of experience in similar roles in complex organizations Available to work on shifts Knowledge of GMP 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, different backgrounds and experiences and provide equal opportunity for all. We are BSP.
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