Industry: Pharmaceutical
Location: Malta
Basis: Full time
Remuneration: Salary Benefits
Main Duties:
- Support RIM Vault and other regulatory systems.
- Manage and maintain vendor contracts (NDAs MSAs SOWs) ensuring timely completion.
- Keep records up to date in trackers product folders and regulatory databases.
- Oversee the artwork review and approval process coordinating with vendors and regulatory teams.
- Assist with internal audits and external inspections.
- Manage the PMC/Commitments and CAPA process for Global Regulatory Affairs.
- Provide metrics to track compliance identify gaps and escalate issues when necessary.
- Handle other regulatoryrelated tasks as needed.
What skills do you need:
- Prior experience in a regulatory affairs function 13 years).
- Scientific degree preferable.
- Fluent in English professionally; other languages advantageous
Eligibility to work in the EU is a must