Job Title: Quality Analyst III
Location: Bangalore, India, 560001
Company: Teva Pharmaceuticals
Job ID: 58698
Who We Are
Teva Pharmaceuticals is on a mission to make good health more affordable and accessible to people around the world. We are the leading manufacturer of generic medicines and produce several products on the World Health Organization's Essential Medicines List. Our work impacts the lives of at least 200 million patients globally every day, and we are always seeking innovative ways to improve healthcare. Join us in making a difference!
The Opportunity
As a Quality Analyst III, you will manage the EMSO Quality System requirements in alignment with Teva's quality standards and regulatory guidelines. This role involves ensuring the continuous implementation, maintenance, and improvement of the Quality Management System (QMS) for the EMSO (Emerging Markets and South-East Asia) APAC region.
How You’ll Spend Your Day
Quality System Management for EMSO:
Ensure the EMSO Quality Management System is in place by implementing and maintaining SOPs (Standard Operating Procedures) related to job functions and ensuring compliance with these SOPs.
Review of Quality Documentation:
Review change controls, batch records, investigations related to deviations and complaints, ensuring they are in compliance with regulatory requirements and timelines.
Review batch manufacturing and packing records along with associated validations and perform periodic batch record reviews.
Cross-Functional Team (CFT) Coordination:
Coordinate within EMSO and other regions to meet business requirements and address any escalations as required.
KPI Metrics:
Ensure that KPI metrics meet the requirements for EMSO Quality, and ensure no overdue QMS elements.
Other Duties:
Perform any other duties as assigned by the supervisor related to Quality Management.
Your Experience and Qualifications
Educational Qualifications:
M. Pharm / M.Sc. (Science)
Experience:
Minimum of 10-12 years of experience in the pharmaceutical industry.
Experience in Operational Quality, including handling Change Control, Deviation, and Complaints.
Knowledge and Skills:
In-depth knowledge of cGMP (current Good Manufacturing Practices) and Quality Management Systems (QMS).
Understanding of pharmaceutical manufacturing and supply chain processes.
Familiarity with Compliance Standards and Regulations applicable to the market.
Strong knowledge of Manufacturing Processes.
Teva’s Equal Employment Opportunity Commitment
Teva is committed to providing equal opportunity in employment without regard to age, race, color, religion, sex, disability, sexual orientation, gender identity, or any other legally protected status. We are proud to be an inclusive employer and believe that diverse perspectives make us stronger.
If you're ready to take on this opportunity to support the EMSO Quality system and make an impact in the pharmaceutical industry, we would love to hear from you!
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