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. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.
B.Pharm, M. Pharm, BSC, MSC Jobs in Teva Pharma
Tevapharm India Hiring For Regulatory Affairs Associate
Tevapharm India is Recruiting for Regulatory Affairs Associate Role . 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. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas. .. Interested and eligible candidates apply online with link provide at bottom and check eligibility before apply and Eligibility details as follows .
Vacancy details :
- Company Name: Tevapharm India
- Location :Navi Mumbai
- Post Name:Regulatory Affairs Associate
- Qualification:B.Pharm,M.Pharm.M.sc
- Experience : 02-05 Years
- No of Vacancies : 10
- Salary:Not Disclosed
Job Description/skills Required:
- Compiling of the Annual Report and ensuring it is submitted prior to the commitment date (at minimum no later than the due date)
- Compilation and submission of post approval supplements (CBE 0, CBE 30, PAS) in US
- Coordinating the retrieval of supporting documentation in accordance with the Annual Report schedule
- Retaining all supporting documentation as required in completing an Annual Report
- Notifying Regulatory Affairs Manager or designee (and Quality, if required) that an Annual Report is at risk of being submitted late
Selection Process: Shortlisted candidates may called for selection process including personal interview and Group discussion ,Exam
How to Apply : Click here for full details and apply
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Teva Pharmaceutical looking for Quality Analyst
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. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.
Post : Quality Analyst III
Job Description
• Preparation of Test Licence and Mfg. Licence, additional Bulk Pack or Blister pack application etc.
• Coordinate and follow up with local FDA for receipt of licence and addressing the queries initiated by Local FDA.
• Preparation of test license NOC for new drugs application.
• Complying any condition mentioned in the import licence and the NOC to DCGI
• Preparation of Import licence for stability and method transfer samples.
• Preparation of test license NOC for new drugs application.
• Complying any condition mentioned in the import licence
• Preparation of application for import & export licence for Narcotic & Psychotropic Substances.
• Complying any condition mentioned in the Narcotic licence
• DATA INTEGRITY COMPLIANCE :
• Handling of training related activities as a TSA (Training system administrator) and Coordinating with other departments
• cGMP trainings to all employees.
• Maintenance of the training records of the employees.
• Responsible for imparting induction training, quality systems training, departmental training and maintenance of training records, Preparation of departmental training schedule.
• Responsible to monitor and to ensure the functioning of Trackwise Training manager at Site.
Candidate Profile
BSc/B Pharm with 9 to 12 years
Additional Information
Qualification : B.Pharm, B.Sc
Experience : 9 to 12 years
Location : Goa
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Quality
End Date : 28th February, 2019
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