Quality Analyst II

Date: May 17, 2024

Location:

Mumbai, India, 400059

Company: Teva Pharmaceuticals

Job Id: 56017

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

The jobholder acts as a member of Teva External Manufacturing & Supply Organization (EMSO)

Jobholder closely interacts with the Team Leader and the QRM’s and if required other departments such as Operations, Procurement, Supply Chain, MS&T, and Regulatory Affairs and provides complete support from quality perspective.

The position is to review the QMS documents like batch records, change controls, deviations, LIR, APR associated with formulations that include various dosage forms of products supplied to EMSO. The market is primarily for US, EU and Canada.

The jobholder will be responsible for review of QMS documents and ensuring that the Supply is not interrupted due to the delay and provides timely updates on the status of the QMS documents.

How you’ll spend your day

To manage the EMSO Quality system requirements in accordance with Teva quality standards and in compliance with the regulatory requirements.

This activity has the following aspects –

• Batch record review and disposition in global system like SAP etc.

• Responsible to follow the Quality Management System of EMSO organisation, which is relevant to the job function

• CAPA management

• Life cycle management of Change control system

• Review of deviations/LIRs

• Review of APRs

• Preparation of Standard Operating Procedure

• Training Management

• Document Management

Your experience and qualifications

Qualification: M/Pharm/ Pharma/ M.Sc. Chemistry

Experience; 6+ years

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

EOE including disability/veteran