PT BrightGene Biomedical Indonesia

PT BrightGene adalah perusahaan farmasi berbasis riset yang bertujuan untuk menjadi yang terdepan sebagai pengembang dan produsen bahan aktif farmasi berkualitas tinggi untuk kebutuhan industri farmasi Indonesia dan untuk ekspor ke pasar ASEAN. Lowongan Kerja PT BrightGene Biomedical Indonesia.

PT BrightGene Biomedical Indonesia adalah perusahaan patungan antara BrightGene Bio-Medical Technology Co., Ltd. (Suzhou) dan tenaga profesional farmasi Indonesia yang berpengalaman. Brightgene Bio-Medical Technology telah berhasil mengembangkan teknologi yang mengurangi risiko, jadwal dan biaya dalam pengembangan obat baik untuk obat inovatif maupun generik serta obat yang menyelamatkan jiwa.

Letak pabrik dibangun di atas lahan seluas 25.000 meter persegi di dalam KNIC, kawasan industri terintegrasi kelas dunia yang dekat dengan Jakarta di Indonesia.

Lowongan Kerja PT BrightGene Biomedical Indonesia

Saat ini PT BrightGene Biomedical Indonesia memberikan kesempatan lowongan kerja untuk dapat bergabung bersama dengan posisi sebagai berikut:

1. Production Supervisor

Requirements :

• Minimum S1 in Pharmacy/ Chemical/ Chemical engineering
• Minimum 2 years experienced from Pharmaceuticals Industry
• English proficiency
• Have a good understanding of the Quality Management System
• Have a good understanding of the production equipment used in the pharmaceutical industry
• Strong leadership skill and analytical thinking

Job Description :

• Supervise related production activities in terms of HSE, Quality and Compliance in the Production area
• Create SOP documents, protocols and reports that are relevant to validation needs, routine activities and each project plan
• Create batch processing and packaging record documents; URS document
• Plan and schedule Operators’ activities
• Coodinate with QA regarding calibration and qualification plans in the Production area

2. QC Microbiology Supervisor

Requirements :

• Bachelor degree of Pharmacy, Chemis, Microbiology, or a related field with 2 years experience in QC Microbiology in Pharmaceutical company.
• Have in-depth knowledge of standard quality control procedures in the GMP/ CPOB corridor for the pharmaceutical industry established by the Ministry of Health and BPOM
• English proficiency (written and oral)
• Have a good understanding of the Quality Management System

Job Description :

• Supervise related laboratory activities in terms of HSE, Quality and Compliance in the QC area
• Create SOP documents, protocols and reports that are relevant to the needs of validation, verification, routine activities and each project plan
• Create specification documents and analysis methods, and URS as needed
• Supervise the use of instruments, equipment, stock materials, reagents, and other consumables; and also ensure its readiness

3. QC Analytical Development Supervisor

Requirements :

• Bachelor degree of Pharmacy, Chemis, Microbiology, or a related field with 2 years experience in QC/ RnD in Pharmaceutical company.
• Have in-depth knowledge of standard quality control procedures in the GMP/ CPOB corridor for the pharmaceutical industry established by the Ministry of Health and BPOM
• English proficiency (written and oral)
• Have a good understanding of the Quality Management System

Job Description :

• Carry out stages of developing API & FDF product analysis methods
• Supervise the development stages of related product analysis methods in terms of HSE, Quality and Compliance in the QC area
• Evaluate the need for use of instruments, equipment, change instrument parts, stock materials and other consumables; and also ensure its readiness
• Coordinate with all departements related to the development stages of analytical methods in the QC area

4. QC Chemical Analyst

Requirements :

• Minimum D3 in Pharmacy/ Chemical
• Minimum 1 year experience in Chemical laboratory
• Good in handling laboratory techniques, research skill, and critical thinking

Job Description :

• Generation of SPOs in relevance with daily routine test and equipment
• Monitoring of stock material, reagents, and consumables
• Preparation and execution of analysis
• Report generation of analysis
• Reception of materials from Warehouse

Tata Cara Melamar:

Apabila berminat dan sesuai dengan persyaratan diatas silahkan lengkapi form pendaftaran melalui link dibawah ini :

DAFTAR

• Hati-hati terhadap segala bentuk jenis penipuan, karena lowongan ini gratis tidak ada biaya dalam bentuk apapun.