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.

How you'll spend your day

Responsible for preparation of Annual quality review /periodic quality review.
Responsible for handling change control system.
Editing & Reviewing of SOP's in Smarteam system
Responsible for the effective implementation of CAPA and to review of CAPA effectiveness.
Responsible for performing ERP/LIMS/SMARTEAM activities which is defined in their privilege.
Responsible for reviewing the executed and master batch card.
Control, distribution & archiving of master documents.
Coordination and review of validation (Process and cleaning) and qualification documentation (Qualification includes all equipment's, facilities, process water,utilities, HVAC and others.
Responsible for coordination in internal as well as in external audits.
Providing cGMP /SOP/General trainings.

JD Contd...

Coordination for technology Transfer/Site transfer documentation for new products
Participation in Internal audit programs to ensure the compliance of quality system.
Responsible for reviewing the investigation initiated due to deviation, OOS, LIR complaints, audits or any incidents. He I She is a part of investigation team.
Responsible for supervising of dispatch activity
Responsible for handling the reprocess, rework, return material.
Coordination for vendor approval procedure
Responsible for supporting to customer experience, Regulatory affairs or other external department requirement.
Responsible for preparation and update of Site Master File and Validation master plan
Responsible for performing quarterly/Periodic trend analysis on Human error, Environment monitoring, Water quality, complaints and others.
Responsible for performing general activity like Mock recall, Shipping validation, Risk assessment and others.

Your experience and qualifications

Education- MSC

Education- 3-5yrs

Already Working @TEVA

If you are a current Teva employee, please apply using the internal career site available on 'Employee Central'. By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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.

Quality Specialist III