Strona główna

In this key position you will support the Microbiological Quality Control Team with knowledge and technical expertise in the field of microbiological techniques and analyzes, as well as transfers and validations of methods, supervising quality investigations and change controls, reviewing and approvals of relevant documentation.

• Development and review of procedures, validation documentation and testing methodology in the field of Microbiological Quality Control
• Development and review of testing strategies and sampling plans in terms of Microbiological Quality Control
• Supervision over the keeping of documentation in accordance with applicable procedures and GMP rules
• Supervision over the implementation and validation of microbiological methods and supporting process validation
• Supervision over the proper performance of microbiological analyzes based on the guidelines of GMP, USP, Eur. Ph., local procedures and specifications in the scope of raw materials, IPC, and finished product
• Supervision over the implementation of the environmental and clean utilities monitoring program in terms of microbiological purity and non-viable particle counting
• Supervision over the quality control of microbiological culture media and disinfectants
• Supervision of the reading and interpretation of the results of microbiological analyzes and of trend analyses
• Performing the function of an administrator of computerized systems for Microbiological Quality Control devices
• Conducting and supervising quality investigations (OOX / DEV / CAPA)
• Initiating and supervising change controls
• Continuous improvement, expanding knowledge through the implementation of the internal training plan and participation in external training
• Participation in internal and external audits and representation of Polpharma Biologics