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

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

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

📌 QA Analyst (Buenos Aires)
🏢 CSL
📍 Buenos Aires