JAMP PHARMA GROUP – We’re Hiring
. 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 Pharmacy / M Pharm
Department: Regulatory Affairs (Canada Market)
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