Tevapharm India is looking to hire Regulatory Affairs Specialist .Interested and eligible candidates can send their resume….Teva Pharmaceutical Industries Ltd., also known as Teva Pharmaceuticals, is an American Israeli pharmaceutical company with dual headquarters in Petah Tikva, Israel and Parsippany, New Jersey, U.S……..The eligibility criteria as follows.
Vacancy details :
|Company Name||: Tevapharm India|
|Designation||: Regulatory Affairs Specialist|
|No. of Vacancies :||:NA|
|Salary||: Not Disclosed|
- -Candidate should have 2-5 years of experience in Regulatory Affairs. -Experienced in Publishing handling US/EU markets. -Experience in ECTD/Insight/IST Tool Box/Lorenz/Adobe Acrobat/Pharmaready publishing tools. -Experience in Submission of dossiers. -Perform document level publishing activities,troubleshoot document issues & perform quality control checks for submission ready documents as per the agency guidance. -Collaborate with scientific personnel for planning,preparation,publishing and quality control checks of publishing.
How to Apply : Click here for full details and Apply