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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
OFFICER FDA (I3CLMG055)
Job Responsibility
- Label Review as per US FDA
- FDA Registrations (Drug, Medical device, Food and Cosmetics)
- Customer comminucation
Candidates Requirements
- Science / Biology Graduates.
- Interested to work from home for Long hours
- Knowledge in MS office
-
Interested in spending long hours in front of a computer
-
Strong in email correspondence
OFFICER - TRAINEE (I3CLMG056)
Job Responsibility
- Learn and Implement specific topics trained in client documentation
- Follow the schedules and requests from higher team members
Candidates Requirements
- Science / Biology Graduates.
- Interested to work from home for Long hours
- Knowledge in MS office
-
Interested in spending long hours in front of a computer
-
Strong in email correspondence
JUNIOR CONSULTANT (Grade 2) (I3CLMG057)
Job Responsibility
- Regulatory documentation for Medical Devices as per EU, UK and FDA Regulation.
- Explain requirements to customers and collect required information on a timely manner.
Candidates Requirements
- Science / Biology Graduates.
- Interested to work from home for Long hours
- Knowledge in MS office
-
Interested in spending long hours in front of a computer
-
Strong in email correspondence
- Knowledge in QA Documentation preferable Pharma / Medical Device.
- Good team player
JUNIOR CONSULTANT (Grade 3) (I3CLMG058)
Job Responsibility
- Regulatory documentation for Medical Devices as per EU, UK and FDA Regulation.
- Explain requirements to customers and collect required information on a timely manner.
Candidates Requirements
- Science / Biology Graduates.
- Interested to work from home for Long hours
- Knowledge in MS office
-
Interested in spending long hours in front of a computer
-
Strong in email correspondence
- Knowledge in QA Documentation preferable Pharma / Medical Device.
- Good team player
SENIOR CONSULTANT (I3CLMG059)
Job Responsibility
- Regulatory documentation for Medical Devices as per EU, UK and FDA Regulation.
- Explain requirements to customers and collect required information on a timely manner.
- Onsite and Offsite customer interactions and meeting
- Weekly project status update
Candidates Requirements
- Science / Biology Graduates.
-
Interested in spending long hours in front of a computer
-
Strong in email correspondence
- Knowledge in MDD/MDR/IVDD/IVDR Technical Documentation.
- Knowledge in ISO 13485 is an added advantage
- Knowledge in Risk Analysis
- Knowledge in Clinical Evaluation is an added advantage
- Good team player
SENIOR ASSOCIATE (I3CLMG060)
Job Responsibility
- Lead a team of 20 members
- Assure NB acceptance of each EU 2017/745 submission.
- Timely completion of projects with limited resources
- Meeting global customers in various countries.
Candidates Requirements
- Pharma or Biomedical professionals
- Minimum 6-8 years of real-time exposure, out of which 2 years as team lead
- Real-world experience interacting with notified Bodies
- Through knowledge in Technical Documentation, standards, risk management and GSPR
- Knowledge in PMS, PMCF, MEDDEV 2.7.1 Revs 4 and 2017/745 Article 61
- Proof of minimum 10 accomplishments in MDD /MDR
- Good Team leader
CUSTOMER RELATIONSHIP OFFICER (I3CLMG061)
Job Responsibility
- Answering to customer enquires and webchat
- Follow up with customers for renewal of EAR, UKRP, FDA Agent renewals
- Develop registration documents and guide customers
Candidates Requirements
- Willing to work long time on computer
- Good team player
- Good communication and email writing skills