The intern will support the Quality Control team in day-to-day laboratory operations, gaining exposure to Good Manufacturing Practices (GMP), analytical testing, and compliance standards in the pharmaceutical industry. This opportunity will provide valuable experience in laboratory procedures, documentation, and quality control processes.

Key Responsibilities:

• Assist with ongoing laboratory operations, including sample program management, document handling, storage, and archiving.

• Support laboratory scientists in routine testing and special projects assigned by management.

• Gain hands-on exposure to quality control testing within an analytical lab setting.

• Observe and learn about sample handling, stability studies, review processes, and metrology.

• Become familiar with Good Manufacturing Practices (GMP) and regulatory compliance standards.

Qualifications & Skills:

• Currently pursuing a Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or a related field.

• Strong understanding of laboratory procedures and quality control principles.

• Basic knowledge of Good Manufacturing Practices (GMP) and regulatory compliance is a plus.

• Proficiency in Microsoft Office Suite (Word, Excel, Outlook).

• Strong organizational skills, attention to detail, and ability to work in a team environment.

Why Join Us?

• Gain hands-on experience in quality control and pharmaceutical laboratory operations.

• Work alongside experienced scientists and industry professionals.

• Develop skills in analytical testing, laboratory documentation, and GMP compliance.