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.

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