Summary:
Dr. Reddy’s Laboratories is seeking a bright and motivated student to join their Regulatory Affairs team for the Summer 2024 internship program. This program offers an invaluable opportunity to gain hands-on experience in ensuring the compliance and approval of pharmaceutical products. You’ll work alongside experienced professionals, contributing to various projects within the regulatory lifecycle of Dr. Reddy’s medications.
Qualifications:
- Currently enrolled in a bachelor’s degree program in life sciences, pharmacy, or a related field (e.g., healthcare administration)
- Strong academic performance in science and regulatory affairs courses (if applicable)
- Excellent attention to detail and accuracy
- Strong research and analytical skills
- Effective communication and interpersonal skills
- Ability to work independently and as part of a team
Responsibilities:
- Assist with research and data collection for regulatory submissions
- Participate in the preparation and review of regulatory documents (under supervision)
- Gain exposure to different regulatory agencies and their requirements
- Learn about Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP)
- Contribute to maintaining regulatory filing timelines and deadlines
- Attend relevant meetings and presentations (as appropriate)
Benefits:
- Competitive hourly wage
- Gain valuable experience in the fast-paced world of pharmaceutical regulations
- Develop skills essential for a career in Regulatory Affairs
- Work alongside industry professionals and gain mentorship
- Network with colleagues across various departments within Dr. Reddy’s
Location
107 College Road East, Princeton, NJ 08540