Regulatory Affairs & Quality Assurance Intern (Uni Undergrad) - Part-Time

About the Role

We 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