Regulatory Affairs Assistant
8 days ago
Plymouth
Regulatory Affairs Assistant Are you ready to take the next step in your career with a vibrant and innovative organisation in the medical device industry? We are seeking a passionate and detail-oriented Regulatory Affairs Assistant to join a dynamic team in Plymouth! This exciting opportunity is perfect for a recent life sciences graduate eager to launch a career in the medical device or pharmaceutical industry and play a meaningful role in creating technologies that genuinely improve patients' lives. About our client: Our client has a strong commitment to quality and innovation, they have a diverse range of products marketed globally. What Will You Do? As a Regulatory Affairs Assistant, your role will be pivotal in ensuring our products meet international regulatory standards. Your responsibilities will include: • Regulatory Submissions: Compile and submit regulatory approvals for various markets, ensuring all documentation is accurate and timely., • Maintain Registrations: Keep current registrations, licences, and certifications up to date, complying with the latest medical device regulations., • Support Audits: Assist with customer audit requests and participate in regulatory authority reviews, preparing necessary documentation and responses., • Collaboration: Work alongside multiple departments, providing regulatory insights and support for information requests., • A science-based degree (or equivalent) or relevant experience in the medical device field, ideally in a regulatory role., • Familiarity with key market approval requirements in APAC, EMEA, and LATAM regions., • Excellent communication skills, both written and verbal, to engage effectively with team members, customers, and regulatory authorities.