Regulated markets and currently working as a shift incharge. Experience in compression, granulation and should possess expertise in Quality Management System (QMS) production.
M.Pharma, M.Sc. in Life Sciences, MBA ; Organizing promotional programs & participation in exhibitions for greater brand visibility including fixing meetings around conferences. Meet, exceed the business closure targets from assigned territory.
Support the implementation of new/revised data systems, technologies, and methods to improve Clario services or support Operation expansion. Participating in systems implementation teams.
Sterile manufacturing Suspension/emulsion /PFS / BFS as well as SKID operation. Should have experience in Aseptic process, complex manufacturing, Exposure to CIP/ SIP SKID, QMS.
Compile registration dossiers for submission to various health authorities like – USA, Canada, Europe, Australia and Israel. Prepare responses to deficiency letters received from various agencies.
Responsible for smoother operation of NMR instruments, shift planning and execution to achieve benchmark productivity month on month basis. Responsible for planning, prioritizing and executing work responsibilities in order to meet deadlines.
For all the positions, it is essential for candidates to have exposure in Injectable Sterile plant and regulatory requirements of documentation as per cGMP/GLP.
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.