Job Description

Position - RA Associate |
Company Name - Abbott Healthcare Pvt Ltd
Website -
Location - Delhi
Work Time -9.00am to 5.00pm
Work Days - Monday to Friday
Week Off - Saturday and Sunday
Salary - Best in Industry
Other benefits- PF, Mediclaim, bonus, days paid leaves.
Minimum Skill, Education, Experience

• Preparation and submission of dossiers for product registrations, import licenses and other approvals from regulatory agencies (registrations and renewals) thereby supporting the business units and supply chain management in compliance with regulatory requirements in the Indian Sub-Continent (India, Sri Lanka, Bangladesh, Pakistan)
• Work with clinical team on submission and approval of clinical trials applications (clinical trial approvals, import licenses/test licenses for clinical trial, amendments, etc.) from various regulatory agencies in the Indian Sub-Continent

• B Pharm / M Pharm / Bachelor or Master Degree in Bio-Medical Engineering / Science discipline with training in Regulatory Affairs
• At least 1 year experience in the pharma/medical device/life science industry in regulatory affairs
• Knowledge in applications of CDSCO

• Excellent communication and interpersonal skills - Good verbal communicator and presenter
• Good verbal and written communication skills in English - with colleagues, management and external authorities
• Be able to plan, manage, organize and report in an efficient way
• Be independent, persuasive, innovative and able to summarize
• Good time management: Well organized, able to set and reset priorities