Qc Analyst

5 months ago


Depok, Indonesia Abbott Laboratories Full time

**No**

**CJR (Core Job Responsibility**

**Actions /Task**

1. Performs Chemical Test Activities
- Perform analysis for incoming material/ Intermediate/ finished product accordingly and generate laboratory worksheets and the report accurately and completely
- Perform chemical testing on stability program
- Record reagents stocks, and make sure all reagents stock is well maintained, and all are within its expiry date.
- Calibrates all of equipment used in lab according to defined schedule.
- Verify Equipment calibration status is available, clear and all are within calibration schedule.

2. Performs Laboratory Function and support
- Ensure that related copy BOP of each laboratory equipment/instrument is available and attached in the related logbook, and ensure all are followed.
- Ensure that laboratory equipment/instruments logbook equipment is filled accurately as per its BOP, completely reviewed and available near to the equipment.
- Perform inspection of laboratory facility related to floors, walls, and ceilings of smooth, hard surfaces that are clean and no deterioration.
- Ensure laboratory housekeeping is well maintained
- Ensure that balance waterpass is in the center position.
- Ensure that all glassware is clean from residue and sticker label.
- Actively involved in maintaining laboratory compliance program in Laboratory
- Ensure laboratory housekeeping is well maintained.
- Actively participated in Continuous Improvement program in Laboratory
- Performs duties as assigned by QC Supervisor or QC Manager effectively and efficiently.
- Participates in investigating any problem and participates in solving out the problem
- Obligates and responsible for good cooperation, work discipline, work safety and safety environment in laboratory, implement and maintain laboratory compliance, keep confidentially of all documents, and achievement on definite yearly goals.

3. Support in Validation Activities in Lab
- Support in performing laboratory test method transfer, test method validation or verification and dissolution profile study as required to fulfill regulatory requirements.


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