Lowongan PT Etana Biotechnologies Indonesia

PT Etana Biotechnologies Indonesia adalah perusahaan bioteknologi terkemuka yang berdedikasi dalam penelitian, pengembangan, dan produksi produk farmasi dan kesehatan berkualitas tinggi. Berlokasi di Kawasan Industri Pulo Gadung, Etana memainkan peran krusial dalam ketersediaan obat-obatan biologis dan vaksin inovatif di Indonesia. Kami menerapkan standar produksi global tertinggi, termasuk cGMP (current Good Manufacturing Practice), untuk memastikan setiap produk aman, efektif, dan memenuhi regulasi kesehatan yang ketat. Inovasi adalah inti dari operasi kami, didukung oleh tim ilmuwan dan profesional yang ahli di bidang bioteknologi, biologi, dan kimia. Etana berkomitmen untuk meningkatkan kualitas hidup masyarakat melalui solusi kesehatan yang berbasis ilmu pengetahuan. Lingkungan kerja kami dinamis, menantang, dan sangat berorientasi pada kualitas dan kepatuhan. Kami menawarkan peluang bagi lulusan baru dan profesional berpengalaman yang ingin berkontribusi pada industri farmasi yang terus berkembang pesat dan berdampak langsung pada kesehatan publik. Kedua perusahaan ini, meskipun di sektor berbeda, sama-sama menawarkan jalur karir yang menjanjikan bagi mereka yang siap berdedikasi dan berprestasi.

ON SITE QA STAFF

JOB SUMMARY

• Conduct real time investigation on site of event, deviation, and other non-conformance to ensure that proper investigation is performed to address the issue.
• Supervise real time in critical production process and in-process control (IPC) activities to ensure activities are conducted in compliance with applicable procedure.
• Perform batch documentation review during process or after process on site to ensure that all products are manufactured in accordance with cGMP and registration dossier.
• Provide real time quality impact assessment of any nonconformance/issue which has potential impact to product quality.
• Perform CAPA Effectiveness check on site.
• Conduct Quality Management System Gap analysis for topic related to Quality Assurance.
• Demonstrate and lead by example for the implementation of Good Documentation Practice.
• Conduct regular oversight with proper evidence.

REQUIREMENTS

• Have min. Bachelor Degree in Biotechnology, Biology, Chemistry. Preferably Pharmacy.
• Have min. 1 year of experience in the Pharmaceutical Industry; fresh graduates are welcome.
• Have good understanding in GMP.
• Excellent skills in prioritizing and time management.
• Fluent in English (both written and spoken).
• Able to work independently (self-motivated) and within a complex team environment.
• Willing to be stationed in East-Jakarta.
• Willing to work with limited resources in a Start-Up Environment.
• Willing to work in shifts.
• Willing to work with overtime if needed.

LOKASI PERUSAHAAN PT. Etana Biotechnologies Indonesia Kawasan Industri Pulogadung Jl. Rawa Gelam V Blok. L Kav. 11-13 Jakarta Timur-13930