Loker jakarta terbaru hari ini pt brightgene biomedical indonesia

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

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