Medical Device Documentation Specialist (m/f/d)
Responsibilities
- Create and maintain technical documentation for medical devices in compliance with MDR
- Support the execution and documentation of PMS activities
- Collaborate with various departments to ensure all regulatory requirements are met
- Monitor and analyze data on product performance and safety post-market
Profile
- Degree in Medical Technology, Engineering, Life Sciences, or a comparable qualification
- Experience in documenting medical devices in accordance with MDR
- Initial experience in Post-Market Surveillance (PMS)
- Knowledge of relevant standards and regulations e.g., ISO 13485, MDR
- Excellent communication skills and the ability to work in an interdisciplinary team
- Detail-oriented and structured working style
- Profound English knowledge, German advantageous
Benefits
- Varied tasks in a renowned international medical device company
- A highly motivated team and an open way of communication
- Remote work possible
About Hays
With over 15 years of experience in the pharmaceutical and chemical industry as well as in 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 experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
Staffing process for freelance specialists
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We carry out a detailed analysis of your technical qualifications on the basis of your CV, your application documents and your profile.
Contact at Hays
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