Semua Label
  • Semua Label
  • BUMN
  • D3
  • FRESH GRADUATE
  • MAGANG
  • S1/S2
  • SMA/SMK

Rekrutment Kandidat PT BrightGene Biomedical Indonesia

Rekrutment Kandidat PT BrightGene Biomedical Indonesia

PT BrightGene Biomedical Indonesia

Detail Pekerjaan

  • PendidikanD3,S1/S2
  • GenderPria/Wanita
  • UmurMaks. 30 tahun
  • Tipe PekerjaanPenuh Waktu
  • Pengalaman2 tahun
  • Diposting
  • Batas LamaranJuli 11, 2024
  • Lokasi KerjaKarawang

Deskripsi Pekerjaan

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
  • GABUNG DI CHANNEL TELEGRAM AGAR TIDAK KETINGGALAN INFO LOWONGAN KERJA TERBARU SETIAP HARINYA KLIK:

    https://t.me/carikarirmu

    (Channel Cari Karirku | Cari Lowongan Kerja)

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