Job
- Level
- Junior
- Job Field
- IT, Security, Test/QA
- Employment Type
- Full Time
- Contract Type
- Permanent employment
- Location
- Frankfurt
- Working Model
- Onsite
Job Technologies
Your role in the team
- Documentation and preparation of information on known medical device risks of the customer.
- Compilation of vigilance data for Periodic Safety Update Reports (PSURs), Post Market Surveillance Reports (PMSR) and Post Market Surveillance Summaries (PMSS).
- Supporting the customer in fulfilling reporting obligations to authorities and notified bodies (vigilance & trend reporting).
- Maintenance of the vigilance databases.
- Creation of further indicators and reports on product quality and product safety.
- Support with the tasks of the Quality Management System such as support with audit preparation.
This text has been machine translated. Show original
Our expectations of you
Education
- Successfully completed studies in the field of natural sciences or a technical training such as MTA / PTA (m/f/d) or comparable qualification.
Qualifications
- Knowledge of EU medical device law and knowledge of the internal and external processes and procedures of the medical device vigilance system is desirable.
- Good MS Office knowledge required.
- Very good written and spoken English skills.
- Basic SAP knowledge desirable.
- Very reliable, careful way of working.
- Confidential handling of information and data relating to product safety.
This text has been machine translated. Show original
Benefits
More net
Health, Fitness & Fun
Work-Life-Integration
Topics that you deal with on the job
Job Locations
This is your employer
FERCHAU Engineering GmbH
Description
- Company Size
- 250+ Employees
- Company Type
- Recruiting Agency
- Working Model
- Full Remote, Hybrid, Onsite
- Industry
- Recruitment Agency