Job Description
Position Overview
We are seeking an experienced RA/PV Manager to lead our Regulatory Affairs and Pharmacovigilance (RA/PV) projects. This key leadership role involves overseeing the execution and delivery of all RA/PV projects, performing quality checks on team output, and managing all regulatory submissions and pharmacovigilance reporting for multiple markets.
Key Responsibilities
- Lead RA/PV projects from initiation to completion, ensuring timely and accurate delivery.
- Draft and compile dossiers for various global markets.
- Perform quality checks on all RA/PV team outputs.
- Manage regulatory submissions and pharmacovigilance reporting for the team.
- Ensure compliance with regulatory authorities across multiple markets.
Candidate Profile
- Education: Master’s degree in Life Sciences, Health, or Biomedical Sciences.
- Experience: 10 to 15 years of experience in Regulatory Affairs and Pharmacovigilance (RA/PV) within regulated markets.
Skills
- Extensive experience across multiple markets, with a deep understanding of regulatory and pharmacovigilance processes.
- Excellent written and verbal English communication skills.
- Proven experience managing and mentoring teams.
- Strong familiarity with submissions to competent authorities.
Benefits
- Competitive remuneration package with regular reviews and salary progression.
- Continuous professional development opportunities in a state-of-the-art, brand-new pharmaceutical facility.
- Comprehensive health insurance.
About Torrent Pharma Malta
Torrent Pharma (Malta) Ltd is a subsidiary of Torrent Pharmaceuticals Limited, one of the leading pharmaceutical companies in India. Having a widespread global presence in over 40 countries, Torrent Pharmaceuticals is deemed as the flagship Company of the Torrent Group.
Torrent Pharma (Malta) was established in 2021 with a strategic purpose to serve as a central hub for Torrent’s sustained growth within the European market. The company fosters an environment where passion meets potential.
