Location: Begumpet, Hyderabad

Qualification: Life science background.

Experience:5-6yrs

JD:

Should be interested to relocate to Hyderabad
Perform quality assurance (QA) activities related to FDA and ROW regulations across therapeutic areas and provide regulatory guidance for all phases of drug development.
Supports the oversight and management of global business partner safety data exchange agreements/pharmacovigilance agreements and other contracts as applicable to ensure compliance with data exchange activity.
Communicates with partner companies and vendors regarding processing and timely exchange of safety data. Distributes aggregate reports as required and assists with reconciliation activities.
Develop/improve and manage quality systems and processes to include;
Creation/revision of appropriate SOPs.

interested candidates kindly call on 9154383165call timings 10:00a.m to 06:00p.m(No Calls on Saturdays and Sundays) or share your resume to hr@mitoconbiopharma.com