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 and approval of method validation protocols and reports Review and approval of method transfer protocols and reports Review and approval of development study protocols and reports Review and approval of equipment instrument calibration and maintenance records Review and approval of equipment instrument validation qualification documentation Review and approval of software validation qualification documentation Review and approval of cleaning validation verification documentation Review and approval of change controls related to SOPs test methods specification documents forms master batch records and master packaging records Review and approval of test methods specification documents SOPs master batch records and master packaging records Review and approval of executed batch records and executed packaging records Review and approval of laboratory test data for raw materials components intermediates and finished products Review and approval of stability data and stability summary reports Review and approval of environmental monitoring data reports and associated documentation QA release of raw materials components and finished product batches Creation of new or revision of existing SOPs Support regulatory external and Teva global audits Support the Inspection Readiness Program Complete training assignments timely by the due date Assist with document number issuance for controlled documents Attend assigned meetings and provide updates as needed Assist with compiling site metrics KPIs and trend reporting Review of environmental monitoring charts and associated documentation Conduct corporate standards gap assessments Support the Vendor Approval Program review of vendor documentation QTAs etc Train and maintain proficiency with computerized systems Glorya Veeva Studium IT systems etc Perform other activities as assigned by the manager Your experience and qualifications Required undergraduate BA BS degree in Life Sciences or related field A minimum of 3-5 Yrs of experience in Pharmaceutical QA GMP environment Equivalent combination of education and or relevant work experience will be considered 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 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 Teva Pharmaceuticals is committed to equal prospect 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

📌 Quality Sr Specialist (Bengaluru)
🏢 Teva Pharmaceuticals
📍 Bengaluru