Intern - Quality Assurance - Oncology

Labcorp•Baltimore, MD

1d•$18 - $20•Onsite

About The Position

Labcorp is seeking a Quality Assurance Intern to join their Quality Assurance Team in Baltimore, MD. This is an 11-week paid internship as part of the Labcorp Global Internship Program, focused on healthcare innovation. Interns will work on impactful projects, gain real-world experience, and support Labcorp's mission to improve health and lives. The role involves working with medical device Quality Assurance and regulatory requirements, assisting with record management, and learning about electronic Quality Management Systems (eQMS).

Requirements

Current enrollment in a Bachelor’s degree program in Life Sciences, Biotechnology or Biomedical Engineering
Interest in quality assurance, and medical devices
Eagerness to learn quality tools and data analysis
Show initiative and the ability to work independently under general supervision
Maintains professionalism, including punctuality and appropriate conduct
Strong communication skills; both written and verbal
Interested in medical device document management systems or a Quality Assurance role.
Ability to create filing systems to manage documents and records.
Attention to detail and organization.
Can handle multiple tasks and projects.
Experience with Microsoft Office tools and ability to learn an eQMS software.
Ability to collaborate with various stakeholders and colleagues in a professional setting.

Nice To Haves

Preferred candidates are rising juniors and seniors (Dec 2027 through June 2029 graduation) who are currently enrolled in a relevant degree program; however, all current students pursuing related studies are encouraged to apply.

Responsibilities

Ensure records are reviewed, organized and made available electronically.
Assist with archiving records from medical device development and production.
Audit historical records to ensure information is organized and available.
Opportunity to develop filing systems and re-organize quality system records.
Learn to create reports from an eQMS (electronic Quality Management System).
Establish electronic indexes and matrices to organize Quality Management System documents so information is readily available.
Become familiar with medical device Quality Assurance and regulatory requirements.
Assist in Quality Assurance projects as needed.
Participate in Post-Market Surveillance data review.
Perform related duties as assigned by supervisor.
Maintain compliance with all company policies and procedure.