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Responsibilities: Under direct supervision, supports Quality Assurance activities to ensure compliance with company and cGMP standards Participates in investigation meetings with responsible department and any required support group(s) Performs inspections and maintains quality records for analysis of raw materials, materials in process, and finished products May conduct internal audits including audits of regulatory submissions Assists in preparation for regulatory and customer inspections and participates in inspections to ensure quality standards Executes training/awareness related to investigation and GMP changes to production teamQualifications: Bachelor degree in a relevant scientific discipline (Pharmacy, Chemistry, Biology, Biochemistry) 0-2 years’ experience working in a cGMP regulated environmentDifferent qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
Our Benefits
We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care 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 CSL Behring.
We want CSL to reflect the world around us
As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.