Polpharma Biologics is a state-of-the-art biological R&D and manufacturing facility, one of the most modern in Europe. We have a fantastic, international team of experienced experts and dynamic young scientists with common goals and values. Biotechnology is our passion.
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
Your responsibilities:
Management of CSV Team & all CSV related matters;
Management of CSV Services;
Management of CS Compliance and continuous inspection readiness program;
Ensure Team growth and knowledge management;
Ensuring Computerized Systems are managed in cGMP compliant manner;
Shape CSV processes in Polpharma Biologics Gdansk and cooperate within global organization for processes harmonization;
Prepare company for inspections and audits within CSV area;
Review, compare & align CSV approach within different projects in Technical Operations, Engineering, QC, R&D and IT.
If you have:
Higher education related to automation, robotics, IT or similar studies;
Knowledge of cGMP and FDA requirements;
Experience in Team and Service Management & Coordination in GxP-regulated environment; CSV, Qualification, Testing hands on experience;
Ability to diagnose and solve problems, good work organization skills, efficient work under pressure;
English fluent;
Experience in automation and IT projects management.
Miejsce pracy: okolice Radzymina (woj. mazowieckie) Nr ref.: AUPR/22 Zakres obowiązków: Samodzielne programowanie automatyki dla potrzeb systemów teletechniki budynkowej oraz dla potrzeb...