-Batch Control and release
-Check and monitor all aspects of GMP and related issues
-Communicate with IRFDA and other foreign authorities as required
-Accompany the auditors during GMP inspections
-Pharm D and/or PhD in Pharmaceutics or related topics
-At least 5 years of experience in Pharmaceutical industry
-Familiar with chemical pharmaceuticals manufacturing and GxPs
-Familiar with international guidelines
-Fluent in English
-Ideal Age Range: 30 - 35
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Since 1994, CinnaGen Co. has invested her resources in production of molecular biology reagents and related technologies that would meet the highest international standards. With such efforts, we have established processes to meet all quality criteria. R&D plays an important role in our policies for advancement. Using our expertise, we are constantly moving towards new products as well as improving the quality of our existing product lines.
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