We are looking for a highly motivated and detail-oriented individual to join our team as a Regulatory Affairs Intern in the Pharmaceutical & Life Sciences industry. The ideal candidate will have a strong foundation in regulatory affairs and a passion for learning and growing with our company.

Roles and Responsibility
Assist in preparing and submitting regulatory documents, such as clinical trial applications and marketing authorizations.
Conduct research and analysis on regulatory requirements and develop strategies to ensure compliance.
Collaborate with cross-functional teams, including legal, quality assurance, and product development, to ensure alignment with regulatory standards.
Develop and maintain relationships with regulatory authorities and respond to queries from regulators.




Stay up-to-date with changes in regulatory requirements and implement updates into processes and procedures.
Provide support for training and educational materials related to regulatory affairs.

Job Requirements
Strong understanding of regulatory requirements governing pharmaceutical products.
Excellent analytical, communication, and problem-solving skills.
Ability to work effectively in a rapid-paced setting and meet deadlines.
Proficiency in Microsoft Office and other software applications relevant to regulatory affairs.
Strong attention to detail and ability to manage multiple tasks simultaneously.
Familiarity with Positive Clinical Practice (GCP) principles and regulations is an asset.

📌 Regulatory Affairs Intern Hyderabad
🏢 Naukri Healthcare Jobs
📍 Hyderabad