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About the Company
Regulatory affairs in a biotech / biopharma company with knowledge of drugs and cosmetics act, GMP, Schedule M and having worked extensively in CDSCO, Local FDA, DCGI, RCGM.
About the Role
Must have faced multiple audits by these agencies. He / she must have experience in filing for all types of application including animal studies, clinical trials, marketing authorizations, manufacturing licenses, export and import licenses, GMP certification etc.
Responsibilities
Qualifications
Required Skills
Preferred Skills
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Manager Regulatory Compliance • Republic Of India, IN