We are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

How you’ll spend your day

Performing Stability analysis .
Performing Method transfer/ Method Validation Analysis.
Calibration and validation of instruments / equipment’s Analysis.
Preparation of Method Transfer Protocols (MTP), Method Transfer Report (MTR), Method of analysis (MTH), Test Data Sheet (TDS) for Stability Analysis and Method transfer / Validation any document related to stability analysis, method transfer / method validation in compliance with current guidelines
Preparation of departmental SOP’s in compliance with current guidelines.
Preparation of validation protocols in compliance with current guidelines.
Entry of stability sample results in LIMS / SAP.
Handling of LSCMS Software

Your experience and qualifications

M.Sc. Chemistry with 1-3 years of experience

How We’ll Take Care of You 

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. 

When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way. 

Reports To

In process of validation

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

Stability Analysis,Method Transfer,Method Validation,Instrument Calibration,Equipment Validation,Protocol Preparation,Report Preparation,SOP Preparation,LIMS Entry,SAP Entry,LSCMS Software Handling,Biopharmaceutical,Quality Control

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 performing stability analysis, method transfer/validation analysis, and calibration/validation of laboratory instruments and equipment. Responsibilities also include preparing various technical documents like protocols, reports, and SOPs in compliance with current guidelines.

Ready to join Teva Pharmaceuticals?

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Frequently Asked Questions

What does a Quality Control Technician II do at Teva Pharmaceuticals?

As a Quality Control Technician II at Teva Pharmaceuticals, you will: the role involves performing stability analysis, method transfer/validation analysis, and calibration/validation of laboratory instruments and equipment. Responsibilities also include preparing various technical documents like protocols, reports, and SOPs in compliance with current guidelines..

Why join Teva Pharmaceuticals as a Quality Control Technician II?

Teva Pharmaceuticals is a leading Pharmaceutical Manufacturing company.

Is the Quality Control Technician II position at Teva Pharmaceuticals remote?

The Quality Control Technician II 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 Control Technician II position at Teva Pharmaceuticals?

You can apply for the Quality Control Technician II 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.