Regulatory Affairs Officer Golden bird international

About Golden Bird International

Job Description

Responsibilities

As a regulatory affairs officer, you'll need to:

• ensure that a company's products comply with the regulations of the regions where they want to distribute them
• keep up to date with national and international legislation, guidelines and customer practices
• respond to queries from medical bodies like the CDSCO,Medicines and Healthcare products Regulatory Agency (MHRA)
• collect, collate and evaluate scientific data from a range of sources
• develop and write clear arguments and explanations for new product licences and licence renewals
• prepare submissions of licence variations and renewals to strict deadlines
• monitor and set timelines for licence variations and renewal approvals
• work with specialist computer software and resources
• write clear, accessible product labels and information leaflets
• plan and develop product trials and interpret trial data
• advise scientists and manufacturers on regulatory requirements
• provide strategic advice to senior management throughout the development of a new product
• project manage teams of colleagues involved with the development of new products
• oversee product trials and interpret trail data
• undertake and manage regulatory inspections
• review company practices and provide advice on changes to systems
• liaise with, and make presentations to, regulatory authorities
• negotiate with regulatory authorities for marketing authorisation
• take part in the development of marketing concepts and approve packaging and advertising before a product's release.