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
- To participate in method development and routine analytical support to pilot and CRD for raw materials, intermediates, in-process samples and drug substance.
- Good knowledge of wet chemistry.
- Familiar with HPLC, UPLC, GC, GCHS, FTIR, PSD, TGA and other analytical techniques.
- Stability studies and Forced Degradation studies for drug substance as per ICH guidelines.
- Calibration and Maintenance of sophisticated Instruments, such as Balance, HPLC, GC, IR, Karl Fischer, Melting point analyzer and Polarimetry.
- Conducting routine analysis of CRD and pilot samples as per set procedures.
- Documentation as per GMP requirements.
- Adhering to safety norms and safe culture in lab.
- To ensure online data compilation and recording to have full compliance.
- To contribute in maintaining analytical laboratory as per the GLP and safety requirements.
- To contribute in providing necessary support to QC during validation batches as well as in routine (Need based in justifiable fashion).
- To support in full-filling the regulatory/customer related tasks related to commercial/pipeline products (as per real need and assigned task).
- To participate in departmental trainings/discussion programs.
- Any other assignments allocated by manager/team leader as per time need.
Your Experience And Qualifications
- MSc. in Organic Chemistry/Analytical chemistry
- Work Experience: Required: 3-5 years
Reports To
Manager Analytical R&D
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: Internal Career Site
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
TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service.
Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market.
