Mantell Associates - Argentina, Quality Control

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...