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 CRD for raw materials, intermediates, in process samples and drug substance. Stability studies and Forced Degradation studies for drug substance as per ICH guidelines. Calibration and Maintenance of sophisticated Instruments, such as HPLC, GC, IR, Karl Fischer and Melting point analyzer Familiar with LCMS/MS, HPLC, GC, GCHS, FTIR, XRD, PSD, DSC and TGA Techniques. 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 as per time need. Expertise in Structure elucidation and Identification and characterization of APIs, known and unknown impurities and intermediates by various spectroscopy techniques Good knowledge of wet chemistry. Conducting routine analysis of CRD samples as per set procedures. Your Experience And Qualifications MSc - Chemistry Exp: 6 to 9 Yrs. 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. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.
