Job Description

Company Info Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with co

Company Info Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth! Carrying out dispensing activities as per applicable procedure and verification of dispensing activities performed by chemistoperator. Carrying out process and sampling activities during the production of Intermediate /API's according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Responsible for verification of parameters / observations recorded in batch cards and other GMP related documents. Filling of all the batch cards (production & cleaning) as per approved instructions and verification of the activities performed by chemistoperator. Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Ensure housekeeping of plant and cleanliness of the equipment, update the equipment, use log and cleaning as per applicable procedure. Preparation of batch card, qualification protocol, report & other GMP related documents. Coordination with safety, QA/QC, SRP and maintenance for shift activities. Issuance of safety permits to carry out maintenance activities in shift. Responsible for issuance of raw materials from store as per production requirement. Storage and labeling as per applicable procedure Qualifications Minimum 15+ years in Pharma function. Any Science Graduate Function Manufacturing Sub Function Manufacturing/Operations 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 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.