1. BSc chemistry or equivalent degree
   
2. Experience in a pharmaceutical/healthcare industry is an advantage.
   

Quality

1. To adhere to procedures on cGMP and GLP and relevant ISO procedures that guide all Q.C. processes.

2. Conduct quality control tests on water, bulk, raw material stability samples, and finished products.

3. Document and prepare reports for all QC activities performed online, and calibrate and maintain laboratory equipment as per the plan.

Technical Work

1. Interpret all documents in QC process, revise and prepare SOPs and COAs as required in the process

2. Work effectively with other analysts and team leaders to achieve shared goals and meet timelines for batch processing and filling process.

3. Participate in OOS, OOT investigation, deviation handling, change control, CAPA closure, and quality risk management for continuous improvement.

4. Participate in training, knowledge sharing, and transfer activities for efficiency and competency.

Reporting & Communication

1. Perform online reporting & keep records.

2. Timely and proper communication with staff at all levels while making critical escalations on time.

Safety

1. Use provided personal protective gear appropriately.

2. Proper communication and handling and investigation of all incidents, near misses and accidents