We are seeking a highly organised and diligent Regulatory Officer to join our team and support the full lifecycle of product registration and compliance.
The ideal candidate will hold a Pharmacy Degree or equivalent, communicate clearly in both Maltese and English, possess strong writing skills, and demonstrate solid computer literacy. In this role, you will be responsible for preparing and submitting regulatory documentation—including initial applications, variations, renewals, responses, PSURs/PBRER, and labelling notifications—ensuring all submissions are delivered on time. You will stay up to date with all regulatory matters, including EU Directives, and maintain meticulously organised records and correspondence, both physical and digital. Close collaboration with the Responsible Person, overseas regulatory counterparts, and the Medicines Authority is key, including attending meetings, seminars, and overseas training when required. Additional responsibilities include performing artwork checks before stock release, creating or verifying labelling materials for over‑labelling, and supporting the Responsible Person with tasks such as tenders, self‑inspections, supplier warehouse checks, transport temperature record reviews, stock movements and returns approvals.
Interested in receiving more information, can do so by contacting marina.pages@reed.com or +356 9908 1461.
