Quality Specialist III
full-time•Mumbai
About this role
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
- Preparation of data migration documents
- Perform source to target data mapping which requires detailed review of Analytical methods, Product Specifications, SOPs, monographs for conducting gap analysis
- Execute data migration design, configuration and validation activities
- Perform data configuration in LIMS software - Laboratory information management system
- Proficiency in MS Excel is required.
- Must be detail oriented, fast learner, Good communication skills, Strong computer skills, preferred fluency in international language and ability to work effectively with international teams.
Your experience and qualifications
- M.Sc. /B.Sc. – Chemistry with 1-2 years’ experience in analytical laboratory in a Pharmaceutical Manufacturing unit
- Preferred: knowledge of LIMS software, Knowledge of SQL/Oracle/SAP
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
Data Migration,Analytical Methods,Product Specifications,SOPs,Gap Analysis,Data Configuration,LIMS Software,MS Excel,Detail Oriented,Fast Learner,Communication Skills,Computer Skills,Fluency in International Language,Teamwork
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 Quality Specialist III will prepare data migration documents and perform source to target data mapping. They will execute data migration design, configuration, and validation activities.
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Frequently Asked Questions
What does a Quality Specialist III do at Teva Pharmaceuticals?
As a Quality Specialist III at Teva Pharmaceuticals, you will: the Quality Specialist III will prepare data migration documents and perform source to target data mapping. They will execute data migration design, configuration, and validation activities..
Why join Teva Pharmaceuticals as a Quality Specialist III?
Teva Pharmaceuticals is a leading Pharmaceutical Manufacturing company.
Is the Quality Specialist III position at Teva Pharmaceuticals remote?
The Quality Specialist III position at Teva Pharmaceuticals is based in Mumbai, India. Contact the company through Clera for specific work arrangement details.
How do I apply for the Quality Specialist III position at Teva Pharmaceuticals?
You can apply for the Quality Specialist III 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.