Ensure that the company s products comply with the regulations of the regions where the company wants to distribute the products 2 Keep up to date with national and international legislation guidelines and customer practices 3 Respond to queries from medical bodies like the Medicines and Healthcare products Regulatory Agency MHRA 4 Develop and write clear arguments and explanations for recent product licences and licence renewals and prepare submissions of licence variations and renewals to strict deadlines 5 Monitor and set timelines for licence variations and renewal approvals 6 Write clear accessible product labels and patient information leaflets 7 Plan and develop product trials and interpret trial data 8 Advise on regulatory requirements provide strategic advice to senior management throughout the development of a new product 9 Involved with the development of new products oversee product trials and interpret trail data 10 Review company practices and provide advice on changes to systems 11 liaise with and make presentations to regulatory authorities and negotiate with regulatory authorities for marketing authorisation 12 Take part in the development of marketing concepts and approve packaging and advertising before a product s release Job Type Full-time Pay 22 000 00 - 35 000 00 per month Work Location In person
📌 Sr. Executive Drug Regulatory Affairs Dra (New Delhi)
🏢 AMINORICH Nutrients
📍 New Delhi
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.