Urgent Opening for RA with Heathcare industry at Mumbai

Job Description:

Designation: RA Associate

Department: Regulatory Affairs

Work location: Delhi

Working Days: Mon - Fri

Work Timings: 9AM -5 PM

Salary: Best in industry (On payroll of Talisman HR)

Detailed Job description-

RA Associate:

• 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

Qualifications & Experience: 

• 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

Attributes:

• 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

 Interested candidates share resume on talent@talismanstaffing.com or whatsapp 9892513409