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.
Qualifications
Education:
High School diploma or GED—Required
Current full-time enrollment in an accredited college or university undergraduate or graduate program—Required
Minimum cumulative GPA of 3.0—Required
Additional Requirements:
Must be at least 18 years old.
Must be legally authorized to work in the United States.
Must commit to the full 10-12-week duration of the internship.
To be considered, candidates must meet all the above criteria.
Seniority level
Internship
Employment type
Full-time
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
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