Teva Pharmaceuticals Hiring Pharmacovigilance Associate II M.Pharm/MDS ,B.Pharm/BDS Apply Now
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!
Job Description
Preparation
of Periodic Drug Adverse Experience Reports (PADERs) submitted to the FDA
Safety
analysis of cases identified in the reporting period for Teva’s FDA approved
products
Preparation
of responses to requests from regulatory agencies, as required
Assurance
that all tasks are performed in line with relevant procedures
Cooperation
with other groups within Teva Periodic Reports and Risk Management Centre, US Pharmacovigilance,
Members of the Global Regulatory Operations Team, Members of the Global
Regulatory Affairs Team, and other relevant groups within and outside of Teva Pharmacovigilance Unit
Training
and mentoring of newcomers, as needed
Responsible
to complete all training and SOP/WI reviews in a timely manner
Qualifications
M.Pharm/MDS
with 4-6 years of experience
B.Pharm/BDS
with 5-7 years of experience
Function Regulatory Affairs
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