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Posted 18 hours ago
Medtech Compliance Consultant
Knightec GroupConsultant in Medtech Compliance
Perks & benefits
Education AllowanceCommissionPaid Leave
Requirements
Engineering degree in relevant field, 2-3 years Medtech industry experience, Knowledge of MDR and ISO 13485
Skills
MDRISO 13485Quality Assurance
About the role
Responsibilities
- Contribute to development and quality assurance of medical devices throughout the product lifecycle
- Work within Design Control, technical documentation, Quality Assurance, and regulatory affairs
- Support customers with quality management systems and regulatory compliance
Requirements
- Engineering degree in biotechnology, medical technology, chemical engineering, or similar
- 2-3 years of experience in medical technology (Design Control, CE marking, QA, or RA)
- Understanding of standards such as MDR, ISO 13485, ISO 14971, and IEC 62304
About the Company
Knightec Group is one of Northern Europe's leading strategic partners in product and digital service development, helping customers transform new technology into real-world solutions.
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Knightec Group · Göteborg