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Posted:2 months ago| Platform: 
Work from Office
Full Time
Role & responsibilities : Assist in developing, implementing, and maintaining the QMS, ensuring compliance with regulations Supporting quality assurance efforts and sound experience in report writing. Experince in GMP & GLP is must Preferred candidate profile : The candidate should be from the Pharmaceuticals / API Bulk Drug Manufacturing Industry with good experience in Regulatory like USFDA, EDQM Perks and benefits : Best in the Industry.
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