Career

Job description:
• creating, checking and approving controlled documents:
- clinical evaluation
- post-market surveillance
- instructions for use
- SOPs, work procedures, forms
• conducting internal audits, preparing and organizing third-party audits
• proposal and control of implementation of corrective measures

We require:
• completed university degree in a medical, technical or humanitarian field
• knowledge of spoken and written English for professional communication
• understanding of quality methods and tools
• knowledge of PC work at a high level (MS Office, ERP)
• knowledge of quality management standards (ISO 9001, ISO 13485)
• knowledge of REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL (EU) 2017/745
• ability and desire to learn new things
• experience in a similar position is an advantage

We offer:
• perspective employment in a stable and prosperous company
• a wide range of company benefits
• work in a pleasant environment
• flexible working hours
• professional growth and education

More information from Mr. Valsa, e-mail: valsa@deymed.com, or use the form below.