About this role
Regulatory Affairs Specialist - Medical Devices at Knok. Location: Matosinhos, Porto, Portugal. Role: Manage regulatory, Prepare documentation, Collaborate teams Requirements: 3-5 years regulatory affairs for medical devices; MDR/CE marking; ISO 13485 knowledge; technical documentation; bilingual Portuguese and English; independent and collaborative work. Category: Quality Assurance Seniority: Mid Level Commitment: Full Time Workplace: Hybrid Languages: Portuguese, English