In this role you are required to solve routine problems, largely through precedent and referral to general guidelines. Your primary interaction is within your own team and your direct supervisor
Curation of specimens, their upkeep and acquiring new specimens for the collections. Lead and participate in collections expeditions in view of expanding existing collections.
The antibody team in involved in engineering and development of antibodies, with a deep focus on reagent quality and specificity. The core activities of team include antibody designing, purification, conjugation and testing of antibodies in a variety of immuno-applications using pioneering tools and technologies.
Post of Technical Assistant who have worked in Pharma industries with knowledge of technical and operational activities. Candidates will co-ordinate plant production activities, distribution activities and also will co-ordinate the procurement of material activates, QA,QC and Bulk Drug Project related activities etc.
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.
You will be a member of a newly established virtual team - EU Submission Hub with colleagues in Denmark, Portugal, Poland and Bangalore focusing on clinical trial submissions in EU. EU Submission Hub is part of Submission Management department, who is responsible for electronic submissions to Health Authorities including New Drug Applications and Life Cycle submissions.
Preparation of quality system related, Instrument operation related SOPs, Specification, STPs, GTPs, raw data sheet, certificate of analysis. Preparation, review, execution of method transfer and method validation protocols and reports etc.
Manipal Academy of Higher Education is a globally engaged institution with active partnership with more than 220 leading universities around the globe. Our relations with institutions, government agencies and organisations in study, research and service provide faculty and students access to world-class institutions, experiences and resources.
As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file.
Candidates with laboratory experience in human cell culture, animal handling and prior knowledge of developing therapeutics for different infectious and non-communicable diseases will be preferred