Our client is a top-notch pharma company committed to solutions to cancer treatment. They pioneer in genetically modified immune cells by using their advanced biotechnology. They are the most fast-growing pharma company in Europe with an international work environment.
You will be carrying out all tasks associated with the manufacture of “supercell” products. You will execute GMP runs in close collaboration with all other departments. By troubleshooting processing and equipment issues, you will improve the operational process every day.
-Perform tasks associated with the manufacture of clinical products. . For example, you will check the quality of blood samples, extract cells from them, grow the supercells that will fight cancer, then send them to the hospital for the patients.
-Collaborate with process development and quality assistance as part of a small team.
-Assist with operating GMP runs to develop standard operating procedures, batch records, deviations, and change controls.
-Improve the work process every day by troubleshooting.
-Make sure the documentation goes well accurately by adhering to SOPs and cGMP regulations.
-MBO or bachelor’s degree in life sciences.
-GMP/ manufacturing experience preferred.
-Previous experience in the cleanroom environment.
-Ability to strictly follow SOPs and cGMP regulations and accurately complete documentation associated with clinical manufacturing.
Are you interested in this or another role? Do not hesitate to contact me by applying for this position.