Qity is seeking a Junior Software Development Engineer to join our team. The successful candidate will work closely with our senior software engineers to design, develop and maintain software applications for medical devices. This is a mostly remote position, with occasional in-person meetings as necessary.

Responsibilities

• Collaborate with the senior software engineers to design, develop and maintain software applications for medical devices.
• Participate in the entire software development lifecycle, from design and implementation to testing and maintenance.
• Ensure that the software applications developed comply with relevant regulations and standards.
• Work closely with cross-functional teams, including quality assurance and regulatory affairs, to ensure compliance with relevant regulations and standards.
• Keep up-to-date with emerging technologies and best practices in software development.
• Develop and maintain accurate and comprehensive software documentation.

Qualifications

• Bachelor’s degree in Computer Science, Information Technology, or a related field.
• Strong understanding of software development methodologies and principles.
• Excellent problem-solving skills and ability to work collaboratively with cross-functional teams.
• Strong communication skills, both written and verbal, to document and report on software design and testing results.
• Familiarity with medical device regulations and standards is a plus.
• Experience with software development in a regulated industry is a plus.
• Ability to work independently and manage multiple priorities in a fast-paced environment.
• Knowledge of programming languages such as JavaScript, Node.js, and Python.
• Strong analytical and problem-solving skills with attention to detail.
• Good communication skills in English; proficiency in Dutch is a plus.
• Ability to work both independently and as part of a team.
• Eagerness to learn and adapt in a fast-paced environment.

At Qity, we are committed to the professional development of our team. The successful candidate will receive comprehensive training and support, gaining valuable skills and experience in various areas of medical device development and regulatory compliance. This role requires regular presence (2–3 days per week) at our office in Erpe-Mere.

If you have a passion for developing medical devices, an eagerness to learn, and a desire to work in a fast growing MedTech start-up, we encourage you to apply for this opportunity.