Quality Assurance and Regulatory Affairs Specialist - Warsaw, Mazowieckie
1 dzień temu
Job summary
The Product Compliance team is responsible for ensuring that medical devices comply with applicable regulatory requirements.Every day we work closely with teams designing and manufacturing both medical devices (hardware) and SaMD (Software as a Medical Device).
Requirements:
- Master's or bachelor's degree – preferably technical (e.g. biomedical engineering) or quality-related
- Minimum 2 years of professional experience in the medical devices industry in a role related to Quality Management System maintenance or Regulatory Affairs
Opis pracy
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