Job Description
Knowledge of ISO +001, ISO 13485, CE, US-FDA (510K), Other Regulatory & CDSCO Guidelines.
Planning, review and submission of Documents as per Country Specific regulatory guideline in medical device registration.
Prepare and maintain technical file and medical device master files as necessary to obtain and sustain product approval.
Keeping records to documents and samples of different Countries.
Co-Ordination with respective
Planning, review and submission of Documents as per Country Specific regulatory guideline in medical device registration.
Prepare and maintain technical file and medical device master files as necessary to obtain and sustain product approval.
Keeping records to documents and samples of different Countries.
Co-Ordination with respective
💡 Quick Summary
Seeking a career-building opportunity? The Jr| Regulatory Affairs Executive position is now open for candidates interested in the BPO Jobs sector. This role in Ahmedabad offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in BPO Jobs is a plus.
