Abbott Hiring for Assistant Manager Regulatory Affairs at Mumbai, India Full Time

1. Review and update the pack inserts from Regulatory perspective of new and existing products.

2. Support in getting timely update, review and approval of prescribing information.

3. Preparation of submissions for Life cycle management for approved products and new product applications for India.

4. Coordinate and participate in preparation of different types of regulatory submissions (e.g new registration and variations) to Health Authorities in Srilanka and Nepal.

5. Coordination with Loan License, Third party manufacturers, Abbott Goa and Abbott Baddi for certificates required by Institutional business, preparation of regulatory documentation applications (non-conviction / marketing and manufacturing / production certificates) for Institutional sales business.

6. Coordinate and participate in preparation of dossiers (site registration, import license) for Abbvie products.

7. General regulatory and maintenance tasks.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email corpjat@abbott.com