. repsonsible for material/plasma/product release, including lot release realted job
. support on the supplier audit and plasma center
. manage relase cycle time.
. reponsible for the material management and releated document update
. Associate's degree in a relevant scientific discipline or equivalent vocational or technical training
. 2-3 years experience including experience in the QC or QA pharmaceutical manufacturing/a highly regulated industry
. Proficiency in MS Office and other relevant software programs
. Knowledge of cGMP standards
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
We encourage you to make your well-being a priority. It's important and so are you. Learn more about at CSL.
About CSL Behring
CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about .
We want CSL to reflect the world around us
As a global organisation with employees in 35+ countries, CSL embraces diversity, equity and inclusion. Learn more about at CSL.
Do work that matters at CSL Behring!
CSL Limited is an Australian multinational specialty biotechnology company that researches, develops, manufactures, and markets products to treat and prevent serious human medical conditions.