Executive- Regulatory Affairs

1 - 5 years

2 - 3 Lacs

Posted:5 days ago| Platform: Naukri logo

Apply

Work Mode

Work from Office

Job Type

Full Time

Job Description

Roles & Responsibilities:

  1. Preparation and timely update of

    Technical Files

  2. Regular updating of the

    Quality Manual

  3. Review and update of all relevant

    Standard Operating Procedures (SOPs)

  4. Review and revision of

    Work Instructions

    as per process requirements
  5. Preparation of

    Marketing Support Documents

    from QA perspective
  6. Review and update of internal

    Formats and Templates

  7. Periodic review and update of

    Site Master Files

  8. Must have working knowledge of

    various audits related to the medical device industry

    , including

    ISO 13485

    , MDSAP, and CDSCO inspections

Mock Interview

Practice Video Interview with JobPe AI

Start Job-Specific Interview
cta

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.

Job Application AI Bot

Job Application AI Bot

Apply to 20+ Portals in one click

Download Now

Download the Mobile App

Instantly access job listings, apply easily, and track applications.

coding practice

Enhance Your Skills

Practice coding challenges to boost your skills

Start Practicing Now

RecommendedJobs for You