About this role
About the RoleWe are looking for a proactive and detail-oriented RAQA Intern to support our Regulatory Affairs & Quality Assurance team from Jul to Dec 2026. This internship offers valuable exposure to medical device regulatory processes, quality management systems (QMS), and post-market surveillance activities within a fast-growing healthcare technology company. This is a full-time, on-site role. Responsibilities• Assist in managing and maintaining documentation and records required for regulatory submissions • Proactively maintain and update regulatory databases in accordance with regulatory requirements • Compile and maintain documentation for post-market vigilance activities • Support the RAQA Manager in CAPA investigations related to customer complaints, recurring non-conformances (NCs), and audit findings, and assist in implementing corrective actions where necessary • Assist in maintaining QMS documentation and records • Provide support for ad-hoc duties and projects as assigned Requirements• Currently pursuing or recently completed a degree • Interest in regulatory affairs and a positive attitude • Strong attention to detail and organisational skills • Good written and verbal communication skills • Proficient in Microsoft Office applications • Ability to work independently and collaboratively in a fast-paced environment What You’ll Gain• Exposure to regulatory and quality processes within the MedTech industry • Hands-on experience with QMS and regulatory documentation • Opportunity to work closely with experienced RAQA professionals • Insight into healthcare technology and medical device compliance processes
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