Pharmacovigilance Specialist II

  Pharmacovigilance

Job title: Pharmacovigilance Specialist II

Company: Teva Pharma

Job description: Who are we? 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 coll

Who are we 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. Join us on our journey of growth! Job Description Processing adverse events reports into Teva’s global safety database: The processing includes Adverse Events coding (in medical dictionary – MedDRA), drug coding in the Company Product Dictionary and WHO DD, seriousness and labeling assessment and submission to health authorities Working in global environment: Interacting with other global PV units and local PV reps. around the world on day to day operations and tracking them until timely closure. Meeting the set threshold for Team KPI’s (Quality, Compliance & Efficiency). Any other task assigned by direct manager and assure that all tasks to perform in line with relevant procedures. Qualifications Bachelor’s degree in life sciences / pharmaceutics / nursing / biology / veterinary medicine with experience in pharmacovigilance, case handling, , familiarity working with safety database. The job role requires excellent interpersonal skills, Accuracy, thoroughness & details orientation along with fluency in both written and spoken English Function Regulatory Affairs Sub Function Pharmacovigilance Reports To In process of validation Already Working @TEVA If you are a current Teva employee, please apply using the internal career site available on ‘Employee Central’. By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

Expected salary:

Location: Bangalore, Karnataka

Job date: Fri, 05 Aug 2022 22:05:19 GMT

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