1. Test of API, according to approved test procedure and specification.
2. Test of Local produced bulk product according to approved test procedure and specification.
3. Test of Stability study sample according to approved test procedure and specification.
4. Test of validation sample according to validation protocol
5. Test of generic sample
6. Perform co-lab study between different lab and different products

1. Perform operation, calibration and maintenance of related analysis instrument according to SOPs
2. Maintenance of instrument logbook
3. Perform IQ/OQ/PQ of instrument
4. Management of consumers in lab

1. Taking samples according to SOPs.
2. Labelling materials according to SOPs.

1. Generate Test procedure and specification according to BHC SOP and Pharmacopoeias (CP, Ph. Eur., JP, USP)
2. Prepare Test procedure and cleaning validation procedure of product.
3. Generate raw data sheet and document list for bulk and validation sample.
4. Management of Chemical reagent
5. Management of Reference substance
6. Prepare IQ/OQ documents for Analytical Equipment

Requirement:

1. Bachelor degree, major in pharmacy or chemistry analysis.
2. At least 2 years work experience; Work experience in pharmaceutical plant or Analytical laboratory is preferred.
3. Knowledge on Analytical instrument such as HPLC, GC is needed.
4. Ability to read English is required (Can read specialized paper and Instrument Operation Manual).
5. Eager to learn;
6. Familiar with Chinese GMP is preferred.
7. Good team work spirit.
8. Computer knowledge is required