Key Responsibilities:

• Review quality dossiers in CTD format for new generic drug submissions.
• Compile responses to deficiencies and manage deficiencies for the product portfolio.
• Compile and review the Quality Overall Summary, Module 1, and Module 3 of all planned submissions.
• Collaborate with cross-functional teams within the organization and third parties.
• Manage a team of associates in their daily roles.
• Prepare and submit due diligence reports to senior management in India and Canada.

Additional Information:

• Department: Regulatory Affairs (Canada Market)
• Experience: 4 – 10 years
• Qualification: B.Pharm / M.Pharm
• Location: Ahmedabad

Application Process:

Interested candidates can send their profiles to sjani@jamppharma.com or apply online through the job posting.

If you need any further assistance or details on how to apply, feel free to ask!