The intern will support the Quality Assurance Department by assisting in stability sample tracking, inventory management, label review, and compliance documentation. This role offers exposure to industry regulations, Good Manufacturing Practices (GMP), and quality control processes while working alongside experienced professionals in a fast-paced pharmaceutical setting.
Key Responsibilities:
Assist in organizing and tracking stability samples according to Standard Operating Procedures (SOPs).
Learn about different types of stability studies (e.g., accelerated, long-term, intermediate) based on storage conditions.
Maintain accurate inventory records of stability samples using both physical logs and digital tracking systems.
Verify sample data for accuracy by cross-checking digital and physical records.
Assist in reviewing product labels and Master Labels to ensure compliance with regulatory requirements, including dosage instructions and safety warnings.
Learn how to create and maintain a database for labeling components using RF Smart software, gaining exposure to inventory tracking integration.
Develop skills in stability sample management, labeling compliance, and database management while ensuring adherence to industry and regulatory standards.
Qualifications & Skills:
Undergraduate or Graduate student currently enrolled in an accredited university/college.
Proficiency in Microsoft Excel and Microsoft Word.
Strong attention to detail and organizational skills.
Basic understanding of mathematical concepts for data accuracy and inventory tracking.
Ability to work independently and collaboratively in a team-oriented environment.
Why Join Us?
Gain real-world experience in quality assurance and regulatory compliance.
Develop skills in stability study management, documentation, and inventory tracking.
Work alongside industry professionals to enhance technical knowledge.
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.
The hourly base salary for this position ranges from $20.00 to $30.00 per hour. Amneal ranges reflect the Company’s good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life’s many other commitments and opportunities.
Seniority level
Internship
Employment type
Full-time
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
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