What are the responsibilities and job description for the 2025 Summer Internship - Quality Management position at Amneal Pharmaceuticals?
Job Description
Join Amneal Pharmaceuticals as a Quality Management Intern and gain hands-on experience working within a fast-paced, regulated environment. This internship offers a unique opportunity to contribute to meaningful projects that support the quality and compliance of our manufacturing operations. You'll work alongside professionals in Quality Management and gain exposure to pharmaceutical standards, systems, and regulatory practices.
Key Responsibilities:
Create product-specific PowerPoint presentations related to Unplanned Deviation and Out-of-Specification (OOS) investigations
Audit investigation report folders for completion and compliance prior to distribution and filing
Maintain and update departmental tracking spreadsheets
Follow up on outstanding documentation required for ongoing investigations
Retrieve, review, compile, and chart batch information to support quality reporting
Assist the Quality Management Investigations Team with various tasks and initiatives
Generate investigative actions as needed
Preferred Majors/Fields of Study:
Sciences
Business
Economics
Information Technology (IT)
Skills:
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
Strong communication skills
Excellent organizational and follow-up abilities
Ability to work independently and as part of a team
Qualifications
Education:
About Us
Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws.
Join Amneal Pharmaceuticals as a Quality Management Intern and gain hands-on experience working within a fast-paced, regulated environment. This internship offers a unique opportunity to contribute to meaningful projects that support the quality and compliance of our manufacturing operations. You'll work alongside professionals in Quality Management and gain exposure to pharmaceutical standards, systems, and regulatory practices.
Key Responsibilities:
Create product-specific PowerPoint presentations related to Unplanned Deviation and Out-of-Specification (OOS) investigations
Audit investigation report folders for completion and compliance prior to distribution and filing
Maintain and update departmental tracking spreadsheets
Follow up on outstanding documentation required for ongoing investigations
Retrieve, review, compile, and chart batch information to support quality reporting
Assist the Quality Management Investigations Team with various tasks and initiatives
Generate investigative actions as needed
Preferred Majors/Fields of Study:
Sciences
Business
Economics
Information Technology (IT)
Skills:
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
Strong communication skills
Excellent organizational and follow-up abilities
Ability to work independently and as part of a team
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
- 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.
About Us
Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws.
