Description of Quality Control Supervisor - PT BrightGene Biomedical Indonesia
Job Description
1. Oversee general laboratory activities, including compliance, laboratory practices, and unconformities found in laboratory area
2. Generate SOPs, protocols, and reports in relevance with the needs of validation, verification, routine activities, and any project plan
3. Generate specifications and analytical methods as per required
4. Generate URS for equipment
5. Monitor stock of material, reagents, and consumables; and procure the items accordingly
6. Manage and schedule the activity of the analysts according to project and routine plan
7. Monitor calibration and qualification schedule and plan in QC area, in coordination with QA
Requirements
1. Minimum Bachelor’s Degree majoring in Pharmacy, Chemistry, Microbiology, or related fields with at least 2 years experience working in the pharmaceutical industry
2. Fluent in English
3. Able to operate computer especially Microsoft office softwares
4. Knowledgeable in GMP, GDP, and GLP
5. Good understanding of laboratory equipment used in pharmaceutical industry, Quality Management System, aseptic techniques (Microbiology Supervisor), analytical method validation and verification concept
6. Have knowledge of Pharmaceutical Health and Safety protocols and regulations, and pharmaceutical industry processes and testing procedures
7. 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
