Hybrid Junior QA/RA Specialist in MedTech Growth
Cassini Technologies, Staten Island, NY, United States
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 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 International MedTech startup with real clinical impact Strong learning and growth opportunities in QA/RA Open, collaborative, and supportive culture Room to grow as the company scales Candidates
already residing in the Netherlands
may be eligible for
visa sponsorship .
#J-18808-Ljbffr
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 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 International MedTech startup with real clinical impact Strong learning and growth opportunities in QA/RA Open, collaborative, and supportive culture Room to grow as the company scales Candidates
already residing in the Netherlands
may be eligible for
visa sponsorship .
#J-18808-Ljbffr