The qualified candidate will work in a cGMP Quality Control Analytical lab.
1. Assist Lab Supervisor or Lab Manager in laboratory investigation in case of out of spec.
2. Develop or revise SOP or monograph in Lab.
3. Perform and review release and stability data (APRR) in Lab.
4. Perform and assess the compendia reviewing.
5. Perform and issue QRM in laboratory.
6. Participates in continuous improvement culture within labs. Utilizes continuous improvement tools such as DMAIC.
7. Familiar with PIC/S, ICH, USP and FDA request for laboratory.

Qualifications

• Chemical Laboratory working experience at least for 5 years is preferred.
• Well computer skill especially for Microsoft Office (Word, Excel, Power point, Access, Visio)
• Fluent English reading and writing, average speaking.
• Pharmaceutical validation and qualification experience is required.
• Knowledge of cGMP, FDA Guidelines, GLP is a plus.
• Laboratory management experience is a plus

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.