Quality Management Specialist
Lead quality excellence in medical innovation!
As a rapidly growing Estonian health tech startup, we are seeking a Quality Management Specialist to ensure regulatory compliance and help bring groundbreaking medical solutions to market.
Your impact
Develop and maintain the Quality Management System (QMS) according to ISO 13485.
Ensure compliance with EU MDR (2017/745), ISO 14971 (Risk Management), and other relevant standards.
Communicate with Notified Bodies (NBs) and organize conformity assessments.
Manage regulatory processes for CE marking and liaise with local authorities for market registrations.
What you bring
Experience with ISO 13485 and EU MDR (2017/745).
Knowledge of CE marking, technical documentation, and Notified Body interactions.
Excellent English skills.
Formal qualification in law, medicine, pharmacy, engineering, or another relevant scientific discipline.
Team player with strong problem-solving skills, precision, and accountability.
Why join us?
✅ Make a real impact
Contribute to groundbreaking medical innovations that improve lives worldwide.
🌱 Grow with industry leaders
Develop your career alongside top experts in science, regulatory, clinical, and business fields.
⚖️ Achieve work-life balance
Enjoy flexible hours and a hybrid work model (2 days in-office, 3 remote).
💰 Unlock attractive perks
Receive a competitive salary (from €3000 gross), sport compensation, and thrive in a supportive international team.
"At Nanordica Medical, we don't have problems—only challenges and ways to improve."
Riste Tamm
Quality Specialist at Nanordica Medical
JOIN US ON A MISSION
To revolutionize wound care. Our innovative nanotechnology helps prevent infections and accelerate wound healing, improving the lives of millions worldwide.
Nanordica Medical's recruitment partner is Brandem.