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Responsible for performing the Quality Control (QC) inspection for raw material, packaging material and consumables that were used for production according to established procedures, and also QC inspection for materials used for research and laboratory (chemical/reagent and consumables). Responsible for performing in-process QC for products according to established procedures and as per the defined production planning schedule, and creating CoA if the testing result meets the defined standard/specification. Perform library preparation, quality control, and sequencing runs using Illumina platforms (e.g., MiSeq, NextSeq, NovaSeq) Responsible for performing analysis for all samples received in the laboratory according to established procedures and as per the defined production planning schedule, and creating reports if the testing result meets the defined standard/specification. Conduct troubleshooting for any issue/problem that might arise during the testing and inspection activity. Responsible for inputting reagent and consumables usage during daily activity and analysis using extensive inventory form, reporting to superior for any issues that happen related to the inventory. Responsible that stock of the material is always available, fresh, no expired material/reagent, and reports immediately for any issue related to material/ reagent/ consumables to QA/LAB Staff and the superior. Responsible for ensuring that the laboratory equipment used is functioning properly and reports to the QA/LAB Staff and direct superior for all issues that arise related to these equipment. Informing QA/Lab Staff regarding the repair, maintenance, and calibration activities, following up on progress to QA/Lab Staff until the activity is completed. Responsible for creating and updating the SOP, WI, WO, FORM, and others related to the document management system, especially in the scope of Operations, if necessary participate in reviewing documents from other functions that relate to the operations. Participate during physical stock (stock opname) of the inventory of the material, monthly basis or as per the schedule set. Ideally, You Would Have Passionate in preserving Indonesia biodiversity through sustainable innovations. Bachelor of Science in Biology, Pharmaceuticals, Chemistry, Chemical/Industrial Engineering or other related major. Having experience at least 1 year as a Research or Lab Analyst, in Quality and Laboratory Management System. Having experience in molecular biology techniques is an added value. Having excellent pipetting skills. Understanding of GMP, GLP, CPOIB, CPAKB, ISO 9001, ISO 13485 and ISO 17025 is an added value. Good computer skills, i.e. experience in Google Workspace (Sheet, Slides & Docs) or MS Office (Excel, Word and PPT). Have high integrity, honesty, dynamic, and excellent attention to detail. Able to work with a team, able to communicate well, and interpersonal skills. Thorough & nimble, finished report within time scheduled. QC Analyst Technical Operations Full-Time Jakarta Share on: The most established precision molecular diagnostics company in Indonesia

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