Location: Netherlands (Hybrid)
Experience level: Junior / Early career
About Cassini Technologies
Cassini Technologies is a fast‑growing MedTech company developing innovative diagnostic and surgical guidance solutions for cataract surgery. Our mission is to improve clinical outcomes and simplify surgical workflows through precision technology. We work at the intersection of engineering, clinical science, and regulatory excellence—and we’re building a diverse, international team to scale globally.
About the role
We’re looking for a Junior QA/RA Officer who is eager to learn and grow in a regulated MedTech environment. In this hybrid role, you’ll support our Quality Assurance and Regulatory Affairs teams by maintaining our QMS, supporting regulatory activities, and helping ensure our medical devices meet global regulatory requirements.
This is an ideal opportunity for someone early in their career who wants hands‑on exposure to QA, RA, audits, and medical device regulations in a high‑paced startup setting.
What you’ll do
- Manage incoming QA/RA requests and track follow‑up actions
- Maintain QMS and regulatory databases and document repositories
- Update procedures, registries, and records
- Ensure documents meet document control requirements
- Enter accurate metadata into electronic systems
- Coordinate document reviews and formal sign‑offs
- Organize and document meetings (Complaints, CAPA, Change Management)
- Support internal and external audits
- Support Design History Files and regulatory submissions
- Assist with global regulatory roadmap activities
- Support other QA/RA tasks as assigned
What we’re looking for
- MBO or HBO degree in Engineering, Law, Science, or a related field
- Strong organizational skills and attention to detail
- Comfortable with Excel and PowerPoint
- Excellent written and verbal English skills
- Eager to learn, proactive, and positive
- Able to manage multiple tasks and large amounts of information
- Passion for quality and doing things right
Nice to have
- Exposure to ISO 13485, ISO 14971, 21 CFR 820
- Experience with medical device registrations in multiple regions
Why join us?
- International MedTech startup with real clinical impact
- Hybrid working model
- Strong learning and growth opportunities in QA/RA
- Open, collaborative, and supportive culture
- Room to grow as the company scales
Visa information
Candidates already residing in the Netherlands may be eligible for visa sponsorship.