The intern will work closely with the Quality Assurance team to support day-to-day operations in a fast-paced distribution center environment. This role will involve assisting with various quality assurance tasks, including document control, metrics reporting, and process review.
Key Responsibilities:
Assist the Kentucky Quality Assurance team with day-to-day tasks, including but not limited to document control, monthly metrics reporting, and review processes for accuracy.
Identify areas for improvement from a quality assurance perspective and assist in developing solutions.
Support quality assurance with diverse projects, gaining exposure to regulatory compliance and CGMP standards in the pharmaceutical industry.
Collaborate with team members in a fast-paced office environment, balancing multiple tasks while maintaining attention to detail.
Develop strong communication skills through writing reports and presenting findings to the QA team.
Qualifications & Skills:
Currently enrolled in a degree program in Biology, Chemistry, Physics, or a related field.
Working knowledge of Microsoft Word and Excel for documentation and data analysis.
Detail-oriented with the ability to multitask and manage time effectively.
Strong verbal and written communication skills, with the ability to convey information clearly and concisely.
Strong analytical and problem-solving skills, demonstrating the ability to identify issues and propose effective solutions.
Ability to work both independently and collaboratively in a team environment.
Why Join Us?
Gain valuable experience in quality assurance within a pharmaceutical distribution center, learning about compliance with CGMP standards.
Develop practical skills in document control, metrics reporting, and quality process improvement.
Work alongside experienced professionals in a dynamic and fast-paced environment.
Contribute to projects that have a direct impact on the quality and compliance of pharmaceutical products.
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
Referrals increase your chances of interviewing at Amneal Pharmaceuticals by 2x
