Responsibilities: • Under limited supervision, supports quality assurance processes to ensure compliance to current Good Manufacturing Practice (cGMP) regulatory guidelines • Samples and inspects material using appropriate tools, methods and protective equipment • Assures materials meet the applicable requirements following Standard Operating Procedures (SOPs) • Follows strict cGMP guidelines in assuring material maintains the safety, identity, strength, quality, and purity • Creates logs and maintains accurate records and documentationQualifications: • High School Diploma or equivalent vocational or technical training; Associate's degree in scientific discipline preferred • 1-2 years' related experience including experience in a regulated environment • Knowledge of cGMP standards • Proficiency in Microsoft Office and QA systemsDifferent qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
TPBN1_UKTJ
QA Associate employer: CSL Behring
CSL is an exceptional employer that fosters a dynamic and inclusive work culture, offering employees the chance to lead innovative projects in regulatory affairs while enjoying the flexibility of a hybrid work model. With a strong commitment to professional development, CSL provides ample opportunities for growth and advancement, making it an ideal place for those seeking meaningful and rewarding careers in the healthcare sector.
