8 oportunidades de empleo para gmp compliance en Argentina actualizadas hoy
trabajos encontrados
Mantell AssociatesA global biosimilars CDMO is seeking a detail-oriented Manufacturing Analyst for their Buenos Aires facility. This role involves supporting production activities, ensuring GMP compliance, and maintaining accurate documentation. Candidates should have experience in a biopharmaceutical manufacturing e
A global biosimilars CDMO is seeking a detail-oriented Manufacturing Analyst for their Buenos Aires facility. This role involves supporting production activities, ensuring GMP compliance, and maintaining accurate documentation. Candidates should have experience in a biopharmaceutical manufacturing e
Mantell AssociatesA global biosimilars CDMO is seeking a detail-oriented Manufacturing Analyst for their Buenos Aires facility. This role involves supporting production activities, ensuring GMP compliance, and maintaining accurate documentation. Candidates should have experience in a biopharmaceutical manufacturing e
Mantell AssociatesA global biosimilars CDMO is seeking a detail-oriented Manufacturing Analyst for their Buenos Aires facility. This role involves supporting production activities, ensuring GMP compliance, and maintaining accurate documentation. Candidates should have experience in a biopharmaceutical manufacturing e
Mantell AssociatesA global biosimilars CDMO is seeking a detail-oriented Manufacturing Analyst for their Buenos Aires facility. This role involves supporting production activities, ensuring GMP compliance, and maintaining accurate documentation. Candidates should have experience in a biopharmaceutical manufacturing e
Mantell AssociatesA leading biosimilars CDMO in Buenos Aires is seeking a detail-oriented GMP Documentation Analyst to join their Quality team. This role involves reviewing and managing GMP documentation to ensure regulatory compliance. The ideal candidate will have experience in the pharmaceutical or biotechnology s
Mantell AssociatesA global biosimilars CDMO is seeking a detail-oriented Manufacturing Analyst for their Buenos Aires facility. This role involves supporting production activities, ensuring GMP compliance, and maintaining accurate documentation. Candidates should have experience in a biopharmaceutical manufacturing e
Mantell AssociatesA leading biosimilars CDMO in Buenos Aires is seeking a detail-oriented GMP Documentation Analyst to join their Quality team. This role involves reviewing and managing GMP documentation to ensure regulatory compliance. The ideal candidate will have experience in the pharmaceutical or biotechnology s
$ 13.910.000 – $ 22.115.000al año
Confianza de la estimación: Baja
Estimación basada en datos de mercado. Los salarios reales pueden variar según experiencia, empresa y ubicación.