Mantell Associates - Argentina

Join a world-class biologics organization in Buenos Aires as a GMP Manufacturing Analyst. This hands-on role requires direct, large-scale biologics production experience for the technical review of batch records. Your deep process knowledge of upstream/downstream operations is key to ensuring GMP...

Join a leading biosimilar developer in Buenos Aires as a Quality Control Consultant. This on-site role requires hands-on review of biological raw data (HPLC, ELISA) in a GMP environment. Ensure data integrity and compliance within a fast-paced biologics manufacturing setting. Ideal candidates hav...

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.