NUSANTICS | Career

Home

Career

QA Analyst

Career

QA Analyst

Your Exciting Role

As a Document Control Officer in the management system, responsible to ensure all documents are systematically filed.
Conduct and follow up activity related to product release procedure, starting from collecting Work Order (WO) and Form (FR) documents, ensure the completeness of these documents, and conduct filing for all documents related to product release procedure.
Follow up the customer complaints progress, starting receiving the customer complaints from BD/Sales/Marketing, support in the CAPA investigations, following up the CAPA action plan, after completed, closing the case with documenting the customer complaints data.
Receive and handle non-conformity and incident that had happened, starting from issuing the CAPA request form, support and participate during the investigation and root cause analysis, following up and monitoring the progress until complete.
Responsible for conducting Quality Assurance and Laboratory activities, including supporting general laboratory necessity for Technical Teams (Operations and R&D Teams).
Creating SOP, WI, WO, FORM, and others related to the document management system, especially in the scope of Operations.
Conduct examination and re-check the stock of materials/reagents/consumables regularly, make sure 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 the superior.
Creating PR, following up the approval process up to receiving the goods, and documenting all documents related to inventory monitoring activities.
Preparing the procurement of tools, equipment, and stationery that are needed in the laboratory.
Creating PR and other forms related to Repair, Maintenance, and Calibration activities, following up the progress (including following up for the approval process and for the repair and maintenance, also a calibration report from vendor), and documenting documents related to these activities.
Conduct physical stock (stock opname) of the inventory for the general laboratory regularly (monthly or as per the schedule set and prepare the stock opname result to the superior).
Create weekly and monthly performance reports for technical operation activities.

The most established precision molecular diagnostics company in Indonesia

Find Us

Mon - Fri: 9 a.m. - 6 p.m.

i3L Campus @ Lvl. 3
Jl. Pulomas Barat No.Kav.88, RT.4/RW.9, Kayu Putih, Pulo Gadung,
Jakarta Timur 13210

hello@nusantics.com

+62 (21) 509 194 30

Home

Career

QA Analyst

Career

QA Analyst

Your Exciting Role

As a Document Control Officer in the management system, responsible to ensure all documents are systematically filed.
Conduct and follow up activity related to product release procedure, starting from collecting Work Order (WO) and Form (FR) documents, ensure the completeness of these documents, and conduct filing for all documents related to product release procedure.
Follow up the customer complaints progress, starting receiving the customer complaints from BD/Sales/Marketing, support in the CAPA investigations, following up the CAPA action plan, after completed, closing the case with documenting the customer complaints data.
Receive and handle non-conformity and incident that had happened, starting from issuing the CAPA request form, support and participate during the investigation and root cause analysis, following up and monitoring the progress until complete.
Responsible for conducting Quality Assurance and Laboratory activities, including supporting general laboratory necessity for Technical Teams (Operations and R&D Teams).
Creating SOP, WI, WO, FORM, and others related to the document management system, especially in the scope of Operations.
Conduct examination and re-check the stock of materials/reagents/consumables regularly, make sure 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 the superior.
Creating PR, following up the approval process up to receiving the goods, and documenting all documents related to inventory monitoring activities.
Preparing the procurement of tools, equipment, and stationery that are needed in the laboratory.
Creating PR and other forms related to Repair, Maintenance, and Calibration activities, following up the progress (including following up for the approval process and for the repair and maintenance, also a calibration report from vendor), and documenting documents related to these activities.
Conduct physical stock (stock opname) of the inventory for the general laboratory regularly (monthly or as per the schedule set and prepare the stock opname result to the superior).
Create weekly and monthly performance reports for technical operation activities.

The most established precision molecular diagnostics company in Indonesia

Find Us

Mon - Fri: 9 a.m. - 6 p.m.

i3L Campus @ Lvl. 3
Jl. Pulomas Barat No.Kav.88, RT.4/RW.9, Kayu Putih, Pulo Gadung,
Jakarta Timur 13210

hello@nusantics.com

+62 (21) 509 194 30

Menu

Find Us

Menu

Find Us