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

Review of quality related analytical documents.
Review and release of stability data in software.
Preparation, review, distribution, retrieval, control and archival of quality documents.
Document management in EDMS
Handling of investigations and CAPA

Your experience and qualifications

Year of experience required for the role: min. 3 years in Quality Control
Preferably candidates familiar in handling Labware LIMS, Trackwise, Glorya etc…
Good communication and interpersonal skills.
Good documentation practices.
Computer literacy.

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.

Other facts

Tech stack

Quality Control,Analytical Documents,Stability Data,Document Management,Investigations,CAPA,Communication Skills,Interpersonal Skills,Documentation Practices,Computer Literacy,Labware LIMS,Trackwise,Glorya

About Teva Pharmaceuticals

Teva Pharmaceuticals is a leading innovative biopharmaceutical company, enabled by a world-class generics business. For over 120 years, Teva’s commitment has never wavered. From innovating in the fields of neuroscience and immunology to providing complex generic medicines, biosimilars and pharmacy brands worldwide, Teva is dedicated to addressing patients’ needs, now and in the future. At Teva, We Are All In For Better Health. To learn more about how we make it happen, visit www.tevapharm.com.

Our community guidelines may be found here: https://www.tevapharm.com/news-and-media/teva-social-media-guidelines/

Please note that adverse effects for any of our products should be reported at: https://www.tevapharm.com/teva-medical-information/report-a-side-effect-form/

Product-specific questions should be directed to Teva or Teva Group subsidiaries in your country. Contact details and Teva's Pharmacovigilance Privacy Policy may be found here:
http://www.tevapharm.com/contact_us/

Team size: 10,001+ employees

Website: http://www.tevapharm.com

LinkedIn: Visit

Industry: Pharmaceutical Manufacturing

What you'll do

The role involves reviewing quality-related analytical documents and stability data, as well as managing quality documents. Additionally, it includes handling investigations and corrective actions.

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Frequently Asked Questions

What does a Quality Sr Specialist do at Teva Pharmaceuticals?

As a Quality Sr Specialist at Teva Pharmaceuticals, you will: the role involves reviewing quality-related analytical documents and stability data, as well as managing quality documents. Additionally, it includes handling investigations and corrective actions..

Why join Teva Pharmaceuticals as a Quality Sr Specialist?

Teva Pharmaceuticals is a leading Pharmaceutical Manufacturing company.

Is the Quality Sr Specialist position at Teva Pharmaceuticals remote?

The Quality Sr Specialist position at Teva Pharmaceuticals is based in Chennai, Tamil Nadu, India. Contact the company through Clera for specific work arrangement details.

How do I apply for the Quality Sr Specialist position at Teva Pharmaceuticals?

You can apply for the Quality Sr Specialist position at Teva Pharmaceuticals directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Teva Pharmaceuticals on their website.