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
