Felix Pharmaceuticals
5 days ago
Primary Job Responsibilities:- Life cycle management of approved drug products (by various regulatory authorities) to ensure that drug product(s) and process remain in compliance as per Agency's post approval guidelines and requirements.- Submission of supplement/variation to different territories by complying necessary regulatory requirement of regulatory authorities such as US, EU, Canada etc.) - To ensure that submission are error free, accurate and do comply as per Agency's guidelines, requirements and internal procedure and checkpoints.- Training to the concern persons per current FDA guidance and other updates. Detailed Job Description- Authoring and review of Supplement submission CBE-30, PAS and Annual reports and life Cycle Management. - Assessment of change controls related to product and process changes to ascertain regulatory filing strategy and data requirement to meet post approval regulatory requirements.- Coordination with concerned stake holders for continuous monitoring of planned/unplanned changes in the product and process after product approval.- Compilation, review and submission of MCSR reports, Submission of drug experience reports (DERs), Submission of labeling changes, Submission of Variations, Submission of CMC supplements, Drug listing and facility registration, etc.- Responding queries raised by Regulatory Agencies to maintain the registration approvals. - Coordination with various departments like Quality Control & Quality Assurance, Production and Stability departments based at R&D, Felix Plant, CRO & CMO site for facilitating the life cycle management of Products. Skills Required- Sound knowledge of regulatory guidelines and life cycle management requirements of various regulatory agencies- Experience of handling the post approval activities with USFDA, EU and Health Canada authorities etc.- Able to work under pressure- Good understanding about the criticality involved in life cycle management of drug products with respect to business and compliance perspective (ref:iimjobs.com)
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Felix Pharmaceuticals
5 days ago
Greater Noida, India Felixvet Full timePrimary Job Responsibilities:- CMC review and submission of drug products to different territories by complying necessary regulatory requirement of regulatory authorities such as US, EU, Canada etc.) - To ensure that CMC submission are error free, accurate and do comply as per Agency's guidelines, requirements and internal procedure and checkpoints.- To...
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Felix Pharmaceuticals
20 hours ago
Greater Noida, India Felixvet Full timeAssistant / Deputy Manager - Administration & Facility The Assistant/ Deputy Manager Administration & Facility Management is responsible for smooth day-to-day administrative operations and end-to-end site management across office and facility premises. The role oversees facilities, vendor management, statutory compliance, security, and utilities to ensure...