Teva Pharmaceutical Industries Ltd. recruitment 2019-Apply online: Teva Pharmaceutical Industries Ltd. is inviting eligible candidates to apply online for the position of Q.A,Q.C.PRODUCTION . Candidates can find their eligibility from below details. Eligible and interested candidates can apply from the source may provided at the bottom of this article. This content to be used only for informational purpose and not responsible for the inaccuracy or deficiency of the provided information.
Qualification:M.pharm or Bpharm
Post Name: Regulatory Affairs Associate
Job Description:The role of the RIM Central Data Services Team is to perform registration data entry operations on behalf of Teva Regulatory functions to ensure that data is entered into Teva’s Global Registration Database in line with the global needs of Teva Regulatory Affairs.He / she would be responsible for completing registration data entry for Teva regulatory files. This will include the procurement of data (acquired from source regulatory documentation such as the Regulatory Dossier) where that data is not readily available from within the data entry process inputs such as reports and related documentation. This will require the ability to identify, locate, and enter all relevant registration data missing from the process inputs (i.e. will involve data enrichment activities, which will require significant levels of regulatory knowledge and experience). He / She will also perform Quality Control (QC) checking of the accuracy and completeness for a defined list of priority/critical attributes that have been procurement and entered into the Global Registration database as part of the RIM Central Data Services operation. The person will possess significant experience of Pharmaceutical Regulatory Affairs, including the pharmaceutical regulatory business processes related to the development and maintenance of a regulatory file through its application/registration lifecycle, including a thorough understanding of global pharmaceutical industry regulatory requirements and guidelines. He / She will complete data procurement and RIM data entry activities, which will require a thorough understanding of the structure, and contents of a regulatory dossier (i.e. will be fluent in navigating and understanding the contents of a regulatory dossier). The process of registration data entry will require a thorough understanding of data structures applicable to registration data, workflows, and data entry Work Instructions.
Salary: Not Disclosed by employer.
No of Vacancy:NA
Opening Date: 24-06-2019
About Company : Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day.