Monday, January 6, 2020

Quality Specialist III Teva Pharmaceuticals Manufacturing Quality Assurance B Pharm

Quality Specialist III Teva Pharmaceuticals Manufacturing Quality Assurance B 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 review of executed Batch Records (BMRs & BPRs) of commercial and non-commercial product batches

Responsible for review of executed process validation protocols and reports of commercial and non-commercial product batches

Responsible for collection of manufacturing and analytical data of commercial batches for trending

Responsible for preparation of Annual Product Review / APQR / PQR

Responsible for trending of stability data for Annual Review

Responsible to coordinate with other departments as per requirements for Batch Records, process validation protocols and reports and Annual Product Reviews

Responsible for review of analytical reports

Requires computer proficiency with comprehensive working knowledge of MS Office products

Qualifications
B Pharm with 2-3 years relevant progressive experience in the USFDA/MHRA approved pharmaceutical company (Oral Solid Dose manufacturing environment)

Experience and knowledge of cGMP and other applicable requirements of quality systems and Data Integrity compliance

Function Quality

Sub Function Manufacturing Quality Assurance

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