Selected intern's day-to-day responsibilities include:

1. Ensure that the organization's Quality Management System conforms to regulatory standards, ISO 13485, and MDR 2017 requirements
2. Ensure effectiveness and implementation of MD-QMS adheres to quality objectives and quality policy
3. Prepare and maintain all the necessary documentation (procedures, formats, and records) as per clauses in ISO-13485, MDR-2017, GSPRs, etc., and other process compliance standards
4. Examine the conformity (all documents for approval must be compliant with all relevant regulations, rules, and standards) and take part in the conformity assessment procedures with the coordination of all concerned departments
5. Be the contact point for colleagues within the company in terms of all questions concerning technical documentation and the approval of medical devices

Skill(s) required

Quality Assurance/Quality Control (QA/QC)

Who can apply

Only those candidates can apply who:

1. are available for full time (in-office) internship

2. have relevant skills and interests

* Women wanting to start/restart their career can also apply.

Perks

Certificate

Letter of recommendation

5 days a week

Number of openings