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 pharmacist

Minimum 5 years' e...