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Responsibilities:
- Assist in implementing and maintaining the documentation system and quality management system;
- Perform routine inspection on products at various stages on the production line to implement the GMP policy;
- Other ad hoc projects as assigned.
Requirements:
- Higher Diploma or above in Pharmaceutical Studies or related discipline;
- Hands-on GMP experience in pharmaceutical industry is preferred;
- Hard working, initiative, able to work under pressure;
- Team player with good interpersonal & communication skills;
- Familiar with MS Office Application and Chinese Word Processing;
- Fresh graduates are also considered.
Interested candidates, please forward your resume in WORD format to
[email protected]
quoting reference 'n0423' in the subject line
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