Abbott is a global healthcare leader helping people live healthier, fuller lives. At our Cimanggis manufacturing site, we are looking for a
QA Operations Staff to support quality assurance activities and ensure compliance across pharmaceutical operations.
Key Responsibilities
- Perform daily QA inspections to ensure compliance with GMP and internal procedures
- Review batch records and support finished product release and shipment
- Prepare Certificates of Analysis (CoA) for local and imported products
- Support internal and external audits, including CAPA implementation and follow‑up
- Participate in investigations and problem‑solving activities related to production and warehouse operations
- Execute release, reject, and hold status for raw materials, intermediates, and finished products
- Maintain retained samples, QA documentation, and records in accordance with quality standards
- Contribute to continuous improvement and quality cost‑reduction initiatives
- Collaborate closely with Production, Engineering, Warehouse, and Distribution teams
Qualifications
- Minimum 1 year of experience in the pharmaceutical industry
- Strong attention to detail and commitment to quality and compliance
- Experience working in a regulated manufacturing environment
- Good communication and cross‑functional collaboration skills
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.