💼 Career
For a Stronger Future with Experts in the Field
👩🔬 Would you like to work with us?
We are looking for dynamic, eager-to-learn, and disciplined team members to collaborate with us in developing professional solutions in the areas of quality, regulation, clinical research, and training within the medical device industry.
At Era Management, we place importance on the following:
- • Proficient in regulations such as ISO 13485, MDR/IVDR, FDA, and SFDA.
- • Able to work in a project-oriented manner
- • Strong written and verbal communication skills
- • Experts who pay attention to detail and are committed to ethical values.
🔍 Open Positions
- • Regulatory Consultant (MDR/IVDR)
- • Clinical Project Manager
- • Quality Systems Specialist
- • Educational Content Developer
- • Technical File Specialist
- • Freelance Instructor / Auditor / Writer
📩 Applications
The following Career Application Form Fill it in
or LinkedIn Visit our page.