Intern - Lab Operations, Compliance and Quality
Teva Pharmaceuticals
Full-time
On-site
West Chester, PA
Operations
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Role Summary
Intern - Lab Operations, Compliance and Quality at Teva Pharmaceuticals. This 12-week program provides hands-on experience in laboratory operations and quality control within the Specialty Bioanalytics department, focusing on regulated sample management in a GLP-compliant environment. Location: West Chester, PA. Schedule: 40 hours/week onsite for 12 weeks. Relocation/housing not provided.
Responsibilities
- Sample Management: observe and learn tasks for regulated studies, including lab manual finalization, sample receipt documentation, handling, storage tracking, and disposal; interact with multiple departments and SB bioanalytical groups; learn archival processes and sample recall/destruction; understand import/export requirements; lead sample reconciliation with study teams.
- Laboratory Operations: assist with maintenance qualification processes for temperature-controlled units; help test new equipment or instruments.
- Quality Control: learn good documentation practices; review work in regulated software (ELN, plate readers, LIMS); perform other duties as assigned.
Qualifications
- Currently enrolled in a bachelor's or master’s program in pharmaceutical sciences, biomedical sciences, chemistry, biology, or a related field.
- Fundamental understanding and experience in a laboratory setting (course-related or internship).
- Strong organization, attention to detail, time management, and interpersonal skills.
- Interest in compliance with regulations.
- Working knowledge of Microsoft 365.