REGULATORY AFFAIRS
ASSISTANT MANAGER
Key Roles:
Finalize the preparation of new drug submissions, deficiencies to regulatory letters
and post approval activities for the given portfolio of products. • Manage a team of Associates on the day to day functioning of the assigned roles.
• Provide leadership and mentoring to the Team Leads and Associates.
⚫ Drafting and reviewing the Quality Overall Summary of all planned submissions. • Working closely with cross functional teams within the organization and third party
teams and maintain good collaboration with all parties for the ongoing projects.
• Prepare and submit due diligence reports of proposed dossiers to Senior Management
in India and Canada.
Experience: 7-10 yrs
Qualification: B.Pharm / M.Pharm
Location: Ahmedabad
Department: Regulatory Affairs (Canada Market)
Send profile at
praval@jamppharma.com
or
Scan the QR Code and Apply online
