VBPL is an ISO 13485:2012 and WHO – GMP certified leading global player in Biopharma sector having more than 15 years of operational experience, situated at Hyderabad. We also have offices located in USA. Innovative, ever motivated Research team and uncompromising manufacturing team in providing quality products are our strengths.
Post : Executive or Sr Exe
Department : Regulatory Affairs, Quality Assurance & Quality Control
No of Vacancies : 20 (RA-5, QA-10,QC-5)
Qualification : M.Pharmacy, B.Pharmacy or M.Sc. (Life Sciences)
Experience : 2 to 6 years Budget- 1.5 to 5 lac
Job Description
1) Manage Regulatory Affairs & Pharmacovigilance.
2) Good in English Communication ( written and oral)
3) To have good knowledge of global and Indian regulatory requirements in Injectable or Biological Division.
4) To prepare dossiers for registration of new Products.
5) To prepare applications and make on line submissions for global as well as local clinical trials DCGI and FDA submissions To give in-house Regulatory Affairs support for Clinical studies. To give inputs for the preparation and submission of dossiers.
Interested candidates can share with the below mentioned mail-id raghu@virchowbiotech.com
Raghurami Reddy Palugulla,
Sr Manager-HR,
Virchow Biotech Pvt Ltd -Hyderabad.
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