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!
Documentation Specialist’s role is to participate in the process of supervision, control and revision of the quality documentation related to the activities carried out in the Microbiological Production Department, in accordance with the GMP rules and FDA requirements.