Nusantics Group
- 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
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