1. Prepares and maintain Process Validation Plan
2. Coordinate with supplier, third party and related departments to ensure that Process Validation is completed in a timely and efficient manner.
3. Prepares and/ or reviews Process Validation related documents, including PV protocol and report, Manufacturing Batch Record, Validation Master Plan etc.
4. Follows the validation policies to perform Process Validation and ensure that their activities are compliant with PIC/s and/or FDA GMP requirements.
5. Conduct investigations, provides technical support and trouble shooting activities related to Product scale-up, Process Validation, and perform optimization for relevant process and procedure.
6. Review technical transfer related document from R&D and provide technical suggestion.
7. Provide training to subordinates regarding Process Validation

Requirements:

1.Bachelor or above in Pharmaceutical or related science subject.
2. 2 years experience on validation in Pharmaceutical Industries.
3. General knowledge of Validation System, Production processes and Equipment
4. Familiar with GMP and PIC/S or FDA is an advantage
6. Good command of both spoken and written English. Cantonese and Mandarin are recommended but not strictly required.

We offer competitive package including public holidays, 5 days work, shuttle bus from Fanling, Tin Shui Wai and Long Ping MTR station, medical insurance, free luncheon and discretionary bonus. Interested parties please send your full resume stating your current and expected salary and date of availability to the Human Resources Department, 

(Data collected will be used for recruitment purpose only)