Contact by email or phone.
Job Responsibilities:
- Management of company controlled documentation
- Administrative support for the quality management system
- Maintenance and updating of procedures, forms, and records
- Preparation of documentation for internal and external audits
- Tracking of non-conformance registers, complaints, and corrective actions
- Coordination of revision schedules, audits, and training sessions
- Support for employee onboarding processes
- Collaboration with and support to the Technical Director/Quality Manager
- Administrative support for MDR processes related to medical devices
- Coordination of administrative tasks across departments
Required Qualifications:
- Minimum secondary education with diploma; preferably technical or business/administrative background
- Excellent organizational skills
- Independence and systematic approach
- Attention to detail and ability to work with documentation
- Advanced proficiency in MS Office
- Ability to prioritize and coordinate multiple tasks
- Communication skills and teamwork
- Active and responsible work attitude
Desirable Qualifications:
- Experience with ISO 9001/ISO 13485
- Experience in a manufacturing company
- Experience in quality or documentation
- Experience with medical devices
- English language proficiency at conversational level
Employee Benefits:
- Full-time employment
- Meal allowance, company phone
- On-site physiotherapy and massage services
- Flexible working hours
- 6 days of sick leave
- Possibility of remote work
- Support of a modern Czech company with international presence
- Pleasant and easily accessible location in Ostrava with parking available
- Friendly team and opportunities for further professional developmentContact by email or phone.
Job Responsibilities:
- Management of company controlled documentation
- Administrative support for the quality management system
- Maintenance and updating of procedures, forms, and records
- Preparation of documentation for internal and external audits
- Tracking of non-conformance registers, complaints, and corrective actions
- Coordination of revision schedules, audits, and training sessions
- Support for employee onboarding processes
- Collaboration with and support to the Technical Director/Quality Manager
- Administrative support for MDR processes related to…
Overview
Type
job
Status
active
Visibility
public
Price
30 000 Kč /month
City
Ostrava
GPS
49.8349139, 18.2820084
Email
Phone
Views
2
Published
25. 5. 2026
Edited
2. 8. 2026
Specifications
Shift
Jednosměnný provoz
Region
Moravskoslezský kraj
Employer
CLINITEX s.r.o.
Open positions
1
Profession
Asistent/ka technického ředitele a systému kvality (QMS/MDR)
Start date
2026-06-01
Salary from
30,000
Salary unit
Kč/měsíc
Contact
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