GMP Production

2 days ago


Tai Po, Hong Kong SAR China Leadingnation Full time

A pharmaceutical manufacturing company in Hong Kong is seeking a dedicated production assistant to develop and maintain the documentation system and ensure compliance with GMP standards. The ideal candidate will hold a Higher Diploma in Science or Engineering and have relevant experience in the pharmaceutical sector. Skills in MS Office and Chinese word processing, as well as strong interpersonal and communication abilities, are essential. The role demands a hardworking, self-motivated individual who can work under pressure and is willing to put in overtime. An attractive remuneration package is offered.#J-18808-Ljbffr


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