What you'll be doing

• Staying up-to-date with changing regulatory requirements and guidelines in the pharmaceutical and medical device industries
• Preparing and submitting regulatory documentation such as marketing authorisation applications, clinical trial applications, and post-approval variations
• Liaising with regulatory authorities to address queries and secure approvals for our products
• Providing regulatory guidance and support to the research and development, manufacturing, and quality assurance teams
• Maintaining comprehensive records and databases to track the regulatory status of our product portfolio
• Identifying and mitigating potential regulatory risks to the business
• Contributing to the development and implementation of regulatory strategies aligned with the company's commercial objectives

What we're looking for

• Pharmacy degree and valid registration as a pharmacis...