Responsibilities:

• Under general direction, supports quality assurance with compliance to GMP regulatory guidelines
• Works with quality assurance staff to ensure inspection procedures are maintained
• Coordinates and maintains documentation of manufacturing procedures, deviations, etc.
• Prepares foreign and domestic protocols and QA release checklists
• Ensures samples are sent according to schedule, processing rejections and maintaining rejection database
• May provide additional administrative support to QA management

Qualifications:
• Associate's degree or equivalent vocational or technical education
• 5+ years' related pharmaceutical experience including 2 years' experience in a regulated environment • Proficiency in MS Office and other relevant software programs

Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.

Our Benefits
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Learn more about how we care at CSL.

About CSL
CSL is a leading integral biotechnology company with a dynamic portfolio of life-saving medicines, including those that treat haemophilia and immune deficiencies, as well as vaccines to prevent influenza. Since our start in 1916, we have been driven by our promise to save lives through innovation. Learn more about CSL.

We want CSL to reflect the world around us
At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL

Do work that matters at CSL

📌 QA Analyst (Argentina)
🏢 CSL
📍 Argentina