Mgr Pharmacovigilance at Teva Pharmaceuticals

Urgent
Posted 4 weeks ago
Bengaluru, Karnataka
Rs15,000 - Rs15,000 per month
Application ends: January 26, 2022
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Job Description

Mgr Pharmacovigilance

Teva Pharmaceuticals

Company Info

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!

MSU, PhV Scientist The main responsibilities of MSU, PhV Scientist are
• Perform signal management activities related to Teva products
•… Prepare and lead cross functional Product Safety Group meeting
• provide medical safety information and assessment associated with marketed products to external and internal Teva stakeholders, including Clinical implications and health hazards associated with quality issues , Responses to Health Authorities, preparation of periodic reports
• Take part in databases search strategy discussions and be responsible for the data retrieval for safety assessment and evaluation
• Contribute safety related input to documents related to Teva products independently
• Take part in preparing & providing training / mentoring to newcomers or other MSU members in different topics as required.

Qualifications
• * Bachelor Degree in Pharmacy
• Very good understanding of medical concepts and Experience in MedDRA and WHO-DD coding.
• At least 8 years’ experience as a Pharmacovigilance scientist
• Good communication skills, analytical capability, writing
• Assertiveness, ability to work under pressure in a stressful environment
• Strong written and verbal English communication skills
• Flexibility to adapt to shifting team priorities
• Advanced knowledge of Microsoft Office platforms
• Ability to work collaboratively and effectively in a global team environment
• Good knowledge of regulations (e.g., FDA, EMA, etc)

Function

Regulatory Affairs
Sub Function

Pharmacovigilance
Reports To

Director
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: Internal Career Site 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