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Hybrid Junior QA​/RA Specialist in MedTech

Job in Netherlands, Pemiscot County, Missouri, USA
Listing for: Cassini Technologies
Full Time position
Listed on 2026-04-23
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • IT/Tech
    Data Analyst, Data Scientist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Hybrid Junior QA/RA Specialist in MedTech Growth
Location: Netherlands

Cassini Technologies is a fast‑growing Med Tech 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 Med Tech 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 Power Point
  • 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 Med Tech 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.

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