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BSP Pharmaceuticals S.p.A is a CDMO dedicated to development and manufacturing for cytotoxic and non-cytotoxic products. The QC Chemical Analyst will perform chemical analysis, operate HPLC/UPLC/U V instruments, and contribute to documentation and data integrity in a cGMP setting.
The role requires a Master’s in Chemistry, 2+ years in a similar environment, GMP knowledge, and English working proficiency. Availability for shifts is essential to support multi-site operations.
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.
We are currently looking for a QC Chemical Analyst - that will mainly ensure:
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 the diversity , the different backgrounds and experiences and provide equal opportunity for all.
We are BSP.