Regulatory Affairs Executive
Job Description
JOB DISCRIPTION ( Drug regulatory affairs ) 1. Drug Regulatory Affairs - Job description \xc3\x98 Prepare CTD, ACTD Dossiers and file regulatory submissions \xc3\x98 Perform assessments of new or revised products \xc3\x98 Manage complaint documentation (including investigation and \xc3\x98 closure) \xc3\x98 Respond to inquiries from regulatory bodies \xc3\x98 Should be technically well versed with requirements for medicines with fare knowledge about medicines, food supplement, \xc3\x98 To Coordinate with relevant department for arranging documents \xc3\x98 To prepare / compile dossier for allocated products / countries \xc3\x98 To coordinate with account department for handling Local FDA fees / transfer of amount for legalization etc \xc3\x98 To coordinate with courier agency for dispatches of dossier /samples \xc3\x98 To make timely entries of submissions / dispatches Qualifications :- \xc3\x98 A bachelor\xe2\x80\x99s degree in B. Pharma \xc3\x98 Experienced with (1 year to 5 yrs) both can apply. \xc3\x98 Excellent communication skills \xc3\x98 Should be aware about Microsoft office [word / Excel/ PPT] - Good in data management Job Type: Full-time Salary: 14,000.00 - 25,000.00 per month Schedule:
- Day shift
- Noida, Uttar Pradesh: Reliably commute or planning to relocate before starting work (Required)
- total work: 1 year (Preferred)
+91 9968996869
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Job Detail
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Job IdJD3211140
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IndustryNot mentioned
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Total Positions1
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Job Type:Full Time
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Salary:Not mentioned
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Employment StatusPermanent
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Job LocationNoida, Uttar Pradesh, India
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EducationNot mentioned
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ExperienceYear