Teva Pharmaceuticals Vacancy for Regulatory Affairs Associate
I 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
They will be responsible for Metrics and Reporting mainly for
EU, but ad hoc Globally and for supporting GRA Compliance.
Work with other members of staff for reporting EU Gx &
Specialties metrics.
Provide ad hoc global or regional reports, as required
GRAP/AQUA data entry
Retrieval and analysis of data from GRAP and AQUA
EU submission fee calculations
Assist with managing GRA’s procedures and learning systems
for SOPs & Work Instructions, including processing through established DMS
and LMS and monitoring of periodic reviews.
The candidate will be expected to work within GRA, liaising
with other business units (eg R&D, portfolio, RA etc) to ensure that all
data is compliant.
They need to be familiar with the IT systems the company uses
in order to retrieve the data efficiently and accurately.
Function
Regulatory Affairs
Qualifications
1-2 Yrs MSc / BPharm with exposure to metrics and reporting mainly for EU.
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