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We are Hiring

Interested in QA /RA documentation and wanted to WORK FROM HOME?

We are in the expansion phase and need more people to support the present team.

Inviting application from Qualified Professionals to fill the below vacancy(s). Interested candidates send details to admin@i3cglobal.com

I3CLMG049 - Jr. Consultant - 2 Posts

Job Descriptions:

Medical Device Technical Documentation as per EU MDR and US FDA 510k  for existing clients.

 

Desired Skills:

  • Science Graduates.
  • Knowledge in MDD/MDR CE Marking or USFDA 510k.
  • Must be a team player.
  • Capable to work long hours in front of computer.

I3CLMG050 Trainee Consultant - 2 Posts

Job Descriptions:

Medical Device Technical Documentation as per EU MDR and US FDA 510k  for existing clients.

 

Desired Skills:

  • Science Graduates.
  • Intrested in QA; Food / Pharma Label Review)

I3CLMG053 Sr. Consultant - 1 Post

Job Descriptions:

Medical Device Technical Documentation as per EU MDR and US FDA 510k  for existing clients.

 

Desired Skills:

  • Science Graduates.
  • with 8+ years experience in active Implant device
  • Through knowledge in EU regulatory compliance.
  • Must be a team player.
  • Capable to work long hours in front of computer.