QA/RA Specialist

Job Title: Quality & Regulatory Affairs Specialist (QA/RA Specialist)

Location: Remote, EU citizenship required (European time zones a must)

Role Description:

Join a fast-growing MedTech startup on a mission to make medical device compliance faster and easier. As a Quality & Regulatory Affairs Specialist, you’ll work hands-on to prepare regulatory submissions, create quality and technical documentation, support clients, and contribute to the development of innovative AI-powered compliance tools.

Sector: Medical Devices, MedTech, AI-driven Regulatory Solutions

Must-Have Skills and Experience:

• Bachelor’s degree in Engineering, Life Sciences, or related field
• 2–4 years’ experience in regulatory or clinical affairs within medical devices
• Hands-on experience preparing technical documentation for EU regulatory submissions
• Solid knowledge of EU MDR (2017/745) and medical dev...