Vacancy
for Regulatory Affairs Associate I Teva Pharmaceuticals MPharm / MSc / Bpharm
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
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.
Qualifications
3-4
Yrs Exp MPharm / MSc / BPharm
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