WRITER

As a Plant Manager, my responsibilities were as follows:
• Amend registration dossiers and submit registration applications and negotiate with governmental authorities.
• Monitor and interpret local regulatory issues and trends that will impact the marketability of company products.
• Provide regulatory and product compliance expertise in the area of advertising and label claims for existing and new products.
• Ensure compliance with pharmacovigilance requirements, provide advice on consumer inquiries and adverse events, and report adverse events both internally and to government authorities.
• Provide technical support to respond to consumer and legal inquiries on regulatory issues for locally marketed products.
• Assist in maintaining and reporting measures of product registration and regulatory compliance performance.
• Assist with local statutory reporting requirements.
• Prepare, maintain and update local product registration and regulatory compliance files.


As a Medical Writer my responsibilities were as follows:

o To write in a world leading provider of scientific, technical and medical information was publishing for the healthcare and pharmaceutical industry?
o Then join this Medical Communications publisher and impress with your excellent medical and technical writing skills and experience.
o To produce timely, high quality written material for publications and client projects. This role will also involve liaison with key opinion leaders, experts and allied healthcare groups to develop an information network that will contribute to strategic projects.

o To present with a Masters or PhD in a Medical/Biological Science with Technical Writing experience with an agency or experience with freelance medical writing projects.

Ensure the registration and regulatory compliance of locally marketed products.