Mantell Associates - Argentina, Buenos Aires, On-site work

Join a global biosimilars CDMO as a GMP Documentation Analyst in Buenos Aires. You will manage critical GMP documents, including SOPs and Batch Records, ensuring cGMP compliance. The role requires proven pharma documentation experience, eQMS knowledge, and strong organizational skills for this on...

Join a global biosimilars CDMO as a Manufacturing Analyst in Buenos Aires. Ensure production excellence and GMP compliance by reviewing Batch Records and QC data. Collaborate cross-functionally to support audits and continuous improvement in a high-performance manufacturing environment.