Profil Perusahaan
PT BrightGene Biomedical Indonesia adalah perusahaan farmasi berbasis riset yang berbasis di Indonesia yang bertujuan untuk menjadi yang terdepan sebagai pengembang dan produsen Bahan Aktif Farmasi (API) berkualitas tinggi untuk kebutuhan industri farmasi Indonesia dan untuk ekspor ke pasar ASEAN.
PT BrightGene Biomedical Indonesia adalah perusahaan patungan yang didirikan pada tahun 2018 antara BrightGene Bio-Medical Technology Co., Ltd. (Suzhou, Tiongkok) dan tenaga profesional farmasi Indonesia yang berpengalaman.
Pabrik ini dibangun di atas tanah seluas 25.000 meter persegi di Karawang New Industrial City (KNIC), kawasan industri terintegrasi kelas dunia yang dekat dengan Jakarta di Indonesia. Teknologi manufaktur API tercanggih yang mengurangi risiko, jadwal dan biaya dalam pengembangan obat telah diintegrasikan ke dalam pabrik kami agar berhasil memproduksi bahan obat generik dan menyelamatkan jiwa untuk Indonesia dan ekspor.
Alamat
Karawang New Industry City, Block B No. 8
Karawang, Indonesia
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PT Brightgene Biomedical Indonesia is hiring:
1. HSE MANAGER
REQUIREMENT
- Min. S1 in K3/ Public Health/ Industry/ other relevant field
- >5 years of experience as SPV/ Ass. Mgr. in the pharmaceutical/ chemical/ relevant industry
- Handling ISO 140001, SMK3 and ISO 45001 English proficiency
- Have knowledge and experience in planning, compiling, assessing, making decisions, and monitoring all activities related to the implementation of HSE policies at the site; evaluate performance security and pest control systems.
- Strong leadership skill and analytical thinking
JOB DESCRIPTION
- Assess and make decisions related to HSE policies, security system and pest control.
- Plan, assess, make decisions and monitor all matters related to budget, documentation and activities related to HSE policies, security system and pest control.
- Assess and make decisions relating to members of the HSE department.
- Evaluate HSE departement in terms of facilities, equipment and human resources then provide recommendations to the Plant Manager.
- Responsible for the implementation of HSE policies in accordance with strict compliance with GMP and HSE regulations with the required time and costs.
- Manage and control the implementation of the ISO 45001 (Occupational Health and Safety Management System) and ISO 14001 (Environmental Management System) in all areas and take necessary actions to improve processes.
2. QC CHEMICAL SUPERVISOR
REQUIREMENT
- Pharmacist with min. 2 years experiences in QC Chemical in the Pharmaceutical Industry
- Have in-depth knowledge of standard QC procedures in the corridors of GMP/CPOB for the pharmaceutical industry stipulated by the Kemenkes and BPOM
- Have a strong understanding of analytical method validation & verification concepts
- English proficiency
JOB DESCRIPTION
- Supervise related laboratory activities in terms of EHS, 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 and URS documents, analysis methods as needed
- Supervise the use of instruments, equipment, stock materials, reagents and other consumables; and also ensure its readiness
- Make a plan and schedule activities for Analysts and Lab Assistants
- Coordinate with QA regarding calibration and qualification plans in the QC area
3. QC CHEMICAL ANALYST
REQUIREMENT
- Vocational School in Pharmacy, Chemistry, Microbiology, Industry, or related fields
- Fresh graduate or experience in laboratory
- Good in handling laboratory techniques, research skill, and critical thinking
JOB DESCRIPTION
- Conducting analysis activities in accordance with scheduling and to be appropriate in terms of HSE, Quality and Compliance in the QC area
- Conduct activities in accordance with analysis methods, SOPs and protocols that are relevant to the needs of validation, verification, routine activities, and each project plan
- Carry out work activities based on routine analysis schedules, project- based, or compliance needs and all applicable GMP documents in the QC area correctly (Right First Time)
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