Rekrutment Kandidat PT BrightGene Biomedical Indonesia

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

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