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!
Management of the Quality Control Bioassay team in the Quality Control department, cooperation with internal and external clients. Motivating employees and supporting them with knowledge and technical expertise in the field of biological techniques and analyzes. Preparation, review and approval of protocols, reports, methods, procedures, instructions and other documents related to Quality Control Bioassay in the Quality Control department. Ensuring that all necessary biological tests are performed and the related records evaluated. Accepting or rejecting tested intermediate, loose and final products, as well as the results of tests carried out. Ensuring that relevant transfers and validations are carried out. Ensuring the maintenance and qualification of rooms and apparatus in the department. Ensuring that initial and further training of staff are conducted and adapted to current needs. Selection and cooperation with contract laboratories. Participation and representation of Polpharma Biologics in internal and external audits. Keeping records in accordance with applicable procedures and GMP rules. Preparation of the annual budget necessary to carry out biological analyzes in accordance with the manufacturing process plan.
