Jr Regulatory Affairs Specialist

IBSAGroup Ltd

Lodi, LO, IT
On-site
Medical device regulatory documentation
International medical device registration
Technical documentation lifecycle management
The role involves collecting and managing technical documentation required to register medical devices internationally

Job Summary

  • The role involves collecting and managing technical documentation required to register medical devices internationally.
  • The incumbent will support audits conducted by various Competent Authorities while ensuring compliance.
  • This position requires evaluating and updating technical documentation to meet the specific needs of different global markets.

Matching Summary

Match Score: 85

The role involves collecting and managing technical documentation required to register medical devices internationally.

Skills & Requirements

Must-have

  • Medical device regulatory documentation
  • International medical device registration
  • Technical documentation lifecycle management
  • Audit support with competent authorities

Nice-to-have

  • Team collaboration skills
  • Activity organization and prioritization
  • Punctuality and precision
  • Organizational flexibility and adaptability

Key Requirements

  • Science degree required
  • Minimum 1 year experience in similar role
  • Fluent English written and oral skills

Work Rights

Not specified

Tailored Resume

Cover Letter