PBSP Pharmaceuticals S.p.A is a CDMO with facilities for development and manufacturing across pre-clinical to clinical and commercial supply, including cytotoxic and high potent oncology drugs. The role focuses on deviations investigations, validation protocol drafting, and audit support to maintain quality standards. /ppThe candidate should possess an MA degree in Chemistry, English working knowledge, and a can-do attitude to work across departments and ensure compliance with SOPs and regulations. /p #J-18808-Ljbffr
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