Are you familiar with upstream processes and eager to make a significant impact in our CDMO facility? If so, we have a position that might be of interest for you! We are currently seeking a new collaborator to join our manufacturing team in ThermoFisher as USP Scientist.
Main areas of responsibility
1. Development of technical/scientific activities
In this role, you will play a pivotal role in the development, optimization, and scale-up of various cell culture and viral vector processes up to GMP manufacturing. you will have the outstanding opportunity to be part of the exceptional development and scientific activities. Working closely with your N+1/Senior Scientist, you will realize the technical program associated with the project. Your responsibilities will include driving the design of technical programs, developing and improving processes for project realization, and generating process mapping. You will also build article codes and BOM vital for the program, ensuring that all elements like consumables, products, and documentation are in place for successful technical implementation. Additionally, you will write checklists, master batch records, and work instructions related to the project, and ensure their accurate follow-up. Your role will involve practical implementation of critical steps in R&D or clinical batches, working in sterile conditions and in BL2, and prioritizing the traceability of operations. You will coordinate line-clearance in R&D and complete checklists according to good documentary practices. In addition, you will perform in-process control tests such as cell count and bio-profile to supervise the processes, analyze results, and prepare client slides with the mentorship of the Senior Scientist. Your ownership will also include writing technical reports, leading quality systems, ensuring compliance with regulatory requirements, and participating in the transfer of R&D processes to clinical production.
Support activities
2.