Teva Pharmaceuticals is hiring B.Pharm,M.Pharm.B.Sc.M.sc.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. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives.. Interested and eligible candidates apply online with link provide at the bottom and check eligibility before apply and Eligibility details as follows:
Vacancy details :
- Company Name: Teva Pharmaceuticals
- Location :Navi Mumbai
- Post Name:Regulatory Affairs Associate
- Qualification: B.Pharm,M.Pharm.B.Sc.M.sc
- Experience :01-03 years of total experienceÂ
- No of Vacancies:Not Disclosed
- Salary:Not Disclosed
Job Description/Skills Required
- Develop labeling documents to ensure alignment with the Reference Listing Drug. This includes QC, proofing, editing and formatting of documents, and coordinating the review and approval of final submission documents with US Labeling Team members.
- Create, revise, and prepare labeling documents needed for full responses to FDA via appropriate filing mode. This includes but is not limited to develpment of content of labeling, side-by-side comparisons and other required submission materials, as necessary.
- Work within the team to proofread established labeling files for content accuracy either manually or by utilizing the electronic proofreading tool TVT.
- Work with US Regulatory Labeling Team to ensure assigned projects are submitted on-time following the eCTD requirements related to labeling.
- Maintain knowledge of US regulations, guidelines, and standard operating procedures applicable to US Gx labeling.
- Work in a team environment with moderate supervision.
- Performs all other job related duties as required by management.
Selection Process:Â Shortlisted candidates may called for selection process including personal interview and Group discussion , Exam
How to Apply :Â Click here for full details and Apply
