Kleva Pharmaceuticals

 ο κάτοχος της θέσης είναι   υπεύθυνος για την υλοποίηση των προγραμμάτων παραγωγής/ συσκευασιας  και τήρησης των αντίστοιχων διαδικασιών  βάσει απαιτήσεων 

Χειριστή/τριας Μηχανής Συσκευασίας/Παραγωγής

We are seeking a detail-oriented QC Analyst to ensure products meet company and industry standards. Responsibilities include conducting tests, analyzing data, and identifying areas for improvement. 

QC Analyst

We are looking for an R&D Analyst to join the team at our Product Development Dpt that will take on a challenging and demanding role with primary objectives the execution of analytical method development and validation/verification.

R&D Analyst

We are looking for a CMS Supervisor  to join the team at our Product Development Dpt that will take on a challenging and demanding role with primary objective the compilation and review of the Common Technical Document (CTD) of pharmaceutical products.