Preparing checklist for all new product filing, collecting, reviewing the data & screening for compilation.Preparation of MIS with regard to filings.Storage & archiving of all data & files pertaining to new product registrations, existing products.Summary
Experience:4 - 5 YearsLocation:Bengaluru/Bangalore, Chennai, DelhiEducation:UG - B.Pharma - Pharmacy,B.Tech/B.E. - Any SpecializationPG - Post Graduation Not RequiredIndustry Type:Pharma/ Biotech/Clinical ResearchRole:Regulatory Affairs MgrFunctional Area:Healthcare, Medical, R&DPosted Date:05 AprDesired Candidate Profile
Candidate must B Pharma/BE BTech & Regulatory exp in regulated markets. Checking/reviewing of documents as per regulatory requirements. Maintenance of lists/documents/records. Co-ordinate with QA/production. Perform as per regulatory filing plan.Job Description
Preparing checklist for all new product filing, collecting, reviewing the data & screening for compilation.Preparation of MIS with regard to filings.Storage & archiving of all data & files pertaining to new product registrations, existing products.Keywords: Regulatory affairs, Manager, Regulatory, Pharma, Healthcare, MedicalCompany Profile
Our client is a reputed Pharmaceutical companyContact Details
Company Name:HRD Global ConsultantsWebsite:Executive Name:kavithaAddress:Not MentionedEmail Address:
4 - 5 Years
Bengaluru/Bangalore, Chennai, Delhi
UG - B.Pharma - Pharmacy,B.Tech/B.E. - Any SpecializationPG - Post Graduation Not Required
Pharma/ Biotech/Clinical Research
Regulatory Affairs Mgr
Healthcare, Medical, R&D
05 Apr
Company Name:
HRD Global Consultants
Website:
Executive Name:
kavitha
Address:
Not Mentioned
Email Address:
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