中山市, 广东省, 中国
Onsite
Tasked with ensuring the product does what it is supposed to do and work with products at all stages of production, from development to testing, and make sure products are safe for consumer.
Review procedure, master batch record , protocols for production
Batch release QA check
Handle deviation, change request, CAPAs
Assist maintenance of QMS
Ensure GMP compliance requirements are applied in production area
• University Degree and Scientific background • Minimum 3 years experience in aseptic pharmaceuticals industry • Good experience in QA and validation • Good communication and interpersonal skill • Fluency in English
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