Teva global pharmaceutical leader Quality Analyst I
B. Pharm / M. Pharm
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
Responsible
for preparation of Hold time study Protocols and Reports and handling overall
Hold Time documentation
Responsible
for preparation of schedule of hold time study samples and related sampling and
handling overall Hold Time activities
Responsible
for Co-ordination with IPQA, Quality Control, Pharmtech, production,
formulation and research development and regulatory affairs for all related and
submission with respect to Hold Time
Study Activities
Responsible
for release of Analytical Reports in SAP R/3 System
Responsible
for Maintenance of reserve sample area and its related documentation
Responsible
for reserve sample management from inward, annual inspection, issuance and
destruction
Responsible
for stability sample management and its related documentation
Responsible
for Monitoring of temperature and humidity of Stability chambers and handling
of Newtronic software
Preparation
of relocation protocols, schedules, Product initiation forms and necessary
documents for transfer
Arrangement
and packing of relocation samples for sample transfer activity
Co-ordination
for providing all the necessary documents and details to stability testing
sites
Responsible
for preparation of related SOP’s
Responsible
for investigation related to the assigned areas
Qualifications
B. Pharm / M.
Pharm with 5- 6 years of experience in Oral Solid Dosage Formulaitons
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