Description

What you'll be doing

- Preparing and submitting registration dossiers for new and existing markets
- Tracking submissions, approvals and renewals across multiple countries simultaneously
- Working with in-country distributors and regulatory authorities to keep things moving
- Monitoring regulatory changes globally and flagging anything that affects market access
- Keeping registration records clean, accurate and audit-ready
- Supporting new product launches from a registration and compliance perspective

Requirements

What we're looking for

- Background in regulatory affairs, life sciences, pharmacy or a related field
- Experience managing product registrations across multiple markets
- Organised, detail-oriented and good at following things through to completion




- Comfortable working with external regulatory bodies and internal teams
- Medical device or food supplement experience a plus
- English essential, additional languages a plus
- Eligible to work in Malta
- Candidates must be based in or relocating to Malta, fully eligibility is required as work permit/sponsorship is NOT provided.

Perks

What we offer

- Competitive salary
- Based at our Malta headquarters with an international team
- Real exposure to global markets and regulatory complexity
- A product that genuinely helps people

📌 Global Market Access Specialist (Tasmania)
🏢 Sasmar Pharmaceuticals
📍 Tasmania