We are looking for a highly skilled and experienced qualified to join our team as a Regulatory Affairs specialist, focusing on DCGI submissions. The ideal candidate will have a strong background in the pharmaceutical industry and experience with regulatory affairs.

Roles and Responsibility
Prepare and submit regulatory documents to DCGI for approval.
Ensure compliance with regulatory requirements and guidelines.
Collaborate with cross-functional teams to meet regulatory needs.
Develop and implement regulatory strategies to achieve business objectives.
Conduct thorough reviews of regulatory documents for accuracy and completeness.
Maintain up-to-date knowledge of changing regulatory requirements and guidelines.

Job Requirements
Robust understanding of pharmaceutical regulations and guidelines.
Experience with DCGI submissions and regulatory affairs.
Excellent communication and collaboration skills.
Ability to work in a fast-paced setting and meet deadlines.
Strong analytical and problem-solving skills.
Proficient in regulatory software and systems.

📌 Regulatory Affairs Professional Dcgi Submissions Mumbai (India)
🏢 Naukri Healthcare Jobs
📍 India