Lowongan PT Anvita Pharma Indonesia

PT Anvita Pharma Indonesia (sebelumnya bernama PT BrightGene Biomedical Indonesia) adalah perusahaan farmasi swasta Indonesia yang berfokus pada penelitian, pengembangan, dan produksi Active Pharmaceutical Ingredients (API) atau bahan baku obat. Perusahaan ini merupakan salah satu pelopor produsen API swasta di Indonesia yang mendukung kemandirian industri farmasi nasional.

Perusahaan bergerak dalam: Produksi Active Pharmaceutical Ingredients (API) atau bahan baku obat. Penelitian dan pengembangan (R&D) obat berbasis molekul kecil. Pengembangan formulasi obat jadi. Layanan Contract Development and Manufacturing Organization (CDMO) untuk industri farmasi. Produksi bahan baku obat untuk kebutuhan Indonesia dan pasar ASEAN.

Anvita mengembangkan API untuk berbagai area terapi, antara lain: Obat kanker (Oncology). Obat antivirus dan anti-TBC. Obat diabetes. Obat hipertensi. Obat penyakit jantung. Obat antitrombotik. Obat asam urat. Obat relaksan otot.

Menjadi perusahaan farmasi berbasis riset yang terdepan dalam mengembangkan dan memproduksi bahan baku obat berkualitas tinggi untuk memenuhi kebutuhan industri farmasi Indonesia dan pasar ASEAN. Nilai-Nilai Perusahaan – Budaya kerja perusahaan menekankan: Kolaborasi. Integritas. Inovasi. Dedikasi. Keunggulan (Excellence). Akuntabilitas.

Anvita Pharma menerapkan budaya kerja yang berfokus pada: Inovasi melalui riset dan pengembangan. Kepatuhan terhadap standar Good Manufacturing Practice (GMP). Kolaborasi lintas tim. Pengembangan kompetensi karyawan. Komitmen terhadap kualitas dan keselamatan produk farmasi.

OPEN POSITION

QC CHEMICAL ANALYST

Requirements:

• Bachelor of Vocational School from Pharmacy/Chemistry/Industry/related fields
• Fresh graduate or ≥ 1 years experience in the field of QC in the Pharmaceutical Industry
• Have deep knowledge of QC in the Pharmaceutical Industry
• Have skill in Standard procedures for analytical (sampling, instrument types, general analysis and documentation of analysis results) in the GMP/CPOB corridor for the pharmaceutical industry set by the Ministry of Health and BPOM; Chemical analysis process in pharmaceutical industry; documentation
• Have skills in using MS. Office & Basic skill in English

Jobdesc:

• Carry out analysis activities in accordance with scheduling and to be compliant in terms of HSE, Quality and Compliance in the QC area
• Conduct activities in accordance with analysis methods, SOP and protocols relevant to validation needs, routine activities, and each project plan
• Using instrumentry, equipment, instrument change parts, stock materials and other consumables according to the needs based on scheduling, and also ensure its readiness
• Documentation of all activities carried out n the QC area.
• Support the audit process of GMP, HSE and other audit carried out at QC area facilities
• Involving participation of Continuous Improvement in QC area
• Fulfilling and improving self competency in QC area
• Support maintain stability between teams and a conductive work environment in the QC are
• Complying regulations related to work safety, and maintain work safety supporting equipment to maintain a safe work environment

MACHINERY TECHNICIAN

Requirements:

• Pendidikan SMK dari jurusan Mesin/ Elektronika/ bidang terkait
• Memiliki pengalaman min. 1 tahun di bidang Maintenance di Industri Farmasi
• Memahami prosedur standar proses perbaikan dan perawatan mesin dalam koridor GMP/CPOB,
• untuk industri farmasi yang ditetapkan oleh Kementrian Kesehatan dan BPOM. Memahami dasar penggunaan software PLC serta aplikasi sejenis yang digunakan di industri farmasi
• Memiliki keahlian dalam pengelasan, instalasi listrik, dan gambar teknik

Jobdesc:

• Melakukan kegiatan perbaikan dan perawatan mesin sesuai dengan penjadwalan dan agar sesuai dalam hal HSE, Kualitas dan Kepatuhan di area Engineering
• Menggunakan mesin, peralatan, change part mesin, stok bahan dan bahan habis pakai lainnya
• sesuai dengan kebutuhan berdasarkan penjadwalan; dan juga memastikan kesiapannya
• Melakukan aktivitas sesuai dengan dokumen, SOP dan protokol yang relevan dengan kebutuhan, kegiatan rutin, dan setiap rencana proyek
• Menggunakan mesin, peralatan, change part mesin, stok bahan dan bahan habis pakai lainnya sesuai dengan kebutuhan berdasarkan penjadwalan; dan juga memastikan kesiapannya
• Melakukan dokumentasi terhadap semua aktivitas yang dilakukan di area Engineering
• Mendukung terlaksananya proses Audit GMP, HSE, dan Audit lain yang dilaksanakan di fasilitas Engineering

QC CHEMICAL SUPERVISOR

Requirements:

• Bachelor Degree of Pharmacy/Chemistry/Industry / related fields
• 2 years experience in the field of QC in the Pharmaceutical Industry
• Have deep knowledge of QC in the Pharmaceutical Industry
• Have skill in Standard procedures for quality control in the GMP/CPOB corridor for the pharmaceutical industry set by the Ministry of Health and BPOM; Quality Management System; GMP [CPOB], GDP [Good Documentation Practice) and GLP [Good Laboratory Practice]; Laboratory equipment/instrument used in the pharmaceutical industry; pharmaceutical chemical analysis; Root cause analysis
• Have skills in using MS. Office & Excellent skill in English
• Have Aphothechary Competency Certificate is a plus

Jobdesc:

• Supervise and evaluate the stages of analysis terms of HSE, Quality and Compliance in the QC Chemical area
• Plan and ensure the use of machines/instruments, equipment, stock materials and consumables required to carry out activities and compliance in the QC Chemical area
• Creates SOPs, protocols, and working instruction that are relevant to validation needs, routine activities, and each project plan
• Create specifications and analysis methods as needed
• Create URS documents as needed
• Supervising the use of machines/instruments, equipment, machines/instruments change parts, stock of
• materials and other consumables, and also ensure its readiness
• Planning and scheduling the activities of the Analyst and Inspectors
• Create, review, assess and determine the impact of proposed changes relating to and relating to products, facilities and machines/instruments in QC Chemical area.
• Coordinate cross-functionally with QA, Production, Engineering, and Supply Chain to ensure effective planning and execution of sampling activities, calibration, qualification, environmental monitoring, as well as maintenance, repair, and spare part management for machines and instruments in the QC Chemical area.