All Jobs By - regulatory-affairs-manager All Jobs By - regulatory-affairs-manager

The candidate must have thorough / relevant experience in RegulatoryAffairs, good understanding of regulations, and hands on expe in filing requirements for DMF\'s, Dossiers for CEP, registrations etc ..

\r\n \r\n Job Role The position is responsible for ensuring timely & high-quality submissions to US & EU markets for various dosage forms in e-CTD format and for driving the projects till approval and also for effective life-cycle management of the regulator ..

 A US Multi National looking for AM RA for US & EU Markets. • TECHNICAL EXPERTISE: . • Products Exposure: • Sterile Dosage Form (Liquid Injectable, Powder for Injection, Ophthalmic Products), Cephalosporin Products • Regulatory Affairs: • Regulat ..

Responsible for regulatory work pertaining to chemical raw materials used & products manufactured\r\nEnsure raw materials & products meet globally accepted regulations\r\nInteract with colleagues in other countries\r\nTo work in a SAP environment ..

Candidate with rich experience in professionally managed Cos is desired. They should be able to deliver results with accuracy. ..

Review and submission of Dossiers, regulatory documents, response to deficiencies and guide team members\r\nwell versed with Post approval,renewal activities /end to end cycle of RA.\r\nExposure to CTD format and hands on experience for ROW Market. ..

Sami Labs is looking for   Designation: General Manager - Regulatory Affairs & Quality Assurance   Experience: 15 to 18 years   Job Profile: Filing registration dossiers for finished pharma products in South East Asia, Russia, CIS, and African Countries. Filin ..

\r\n \r\n Designation : Senior ManagerRegistration Location : Mumbai Key Skill : Senior Manager Registration Education : M Sc(Agriculture) Exp : 5 - 10 (Yrs.) Job Profile: \r\nPreparation of dossiers for Patented and Generic products. \r\nPlanning for new products reg ..

The candidate must have thorough / relevant experience in RegulatoryAffairs, good understanding of regulations, and hands on expe in filing requirements for DMF\'s, Dossiers for CEP, registrations etc ..

\r\n \r\n Job Role The position is responsible for ensuring timely & high-quality submissions to US & EU markets for various dosage forms in e-CTD format and for driving the projects till approval and also for effective life-cycle management of the regulator ..

 A US Multi National looking for AM RA for US & EU Markets. • TECHNICAL EXPERTISE: . • Products Exposure: • Sterile Dosage Form (Liquid Injectable, Powder for Injection, Ophthalmic Products), Cephalosporin Products • Regulatory Affairs: • Regulat ..