Documentation preparation like BMR, BPR, Protocols, Reports, etc. required for execution
Preparation & execution of Transfer strategies for scale up batches, transfer batches with proper documentation for new launch / validation batches
To support and coordinate cross functional teams i.e. with QA, QC, Production, warehouse & Purchase department for completion of Site transfer, New product and Alternate source products in a cost effective manner
To support the Regulatory Affairs department for submission.
Preparation of SOPs for departmental functioning
To review the site transfer documents & to communicate with sending site to fulfil the requirements of site transfer projects
Follow up for licensing information for manufacture of drug product, import of drug substance and drug product related to site transfer projects
To complies with GMP and safety procedures in working area
Handling of Trackwise & SAP
Experience of handling of change control, Investigation, CAPA, Deviations and OOS
Qualifications : Master of pharmacy/Bachelor of pharmacy with 3-4 years expereince
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.
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