Project Support Medical Device Regulation for irrigation solutions (m/f/d)
Your responsibilities
- MDR Remediation of design documentation for Irrigation Solutions (different combinations of 8 solutions and 8 containers)
- Gathering of exiting development documentation, currently not included in Technical File, from different client locations
- Detailed review of documents with respect to availability and state-of-the-art, gap analysis
- Support in development of a modular design documentation ? Harmonization of existing design documents (including risk analyses) and closing of identified gaps
Your profile
- Experienced in Product Development of sterile single-use Medical Devices, preferably in the field of Irrigation Solutions
- Experienced in Risk Management o Experienced in writing of design documentation, also in electronic systems
- Profound knowledge of regulatory and normative requirements (MDR, ISO 13485:2016, ISO 14971:2019, IEC 62366)
- Good communication and team skills
Your benefits
- Working in an international company
About Hays
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
Staffing process for a permanent or temporary position
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We will review your application documents and carry out a detailed analysis of your professional qualification.
Your contact at Hays
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