Description of Analytical Development Supervisor - PT BrightGene Biomedical Indonesia

Job Description
1. Coordinate with the Sending Unit/ partner for new products and/or product development
2. Create protocols and reports that are relevant to the needs of validation, verification, and each project plan
3. Create URS for equipment
4. Monitor the stock of materials, reagents and consumables; and obtain the appropriate items, especially for the purposes of validation, verification, and each project plan
5. Manage and schedule the activities of the analysts according to the project, in coordination with the QC supervisor (routinely)
6. Oversee general laboratory activities, including compliance, laboratory practices, and non-conformances found in laboratory areas

1. Pharmacists/ Bachelor of Pharmacy/ Chemistry or related major with at least 2 years experience working as QC or R&D in the pharmaceutical industry/ FMCG
2. Fluent in English
3. Able to operate computer especially Microsoft office softwares
4. Have knowledge about GMP, GDP, and GLP, HSE protocols and regulations, pharmaceutical industry processes and test procedures
5. Good understanding of laboratory equipment used in the pharmaceutical industry, Quality Management System, validation of analytical methods and the concept of verification
6. Willing to work in West Karawang

Job Detail
1. Placement location in Karawang New Industry City, Trans Heksa
2. Pharmaceutical company that aims to be at the forefront as a developer and producer of high quality active pharmaceutical ingredients (API)
3. 3 month probation period

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