Intern - Lab Operations, Compliance and Quality

Role Summary

Intern - Lab Operations, Compliance and Quality at Teva Pharmaceuticals. 12-week program focused on regulated sample management within the Specialty Bioanalytics department, offering exposure to laboratory operations and quality control in a GLP-regulated environment.

Responsibilities

• Sample Management
  • Observe and learn tasks and responsibilities for regulated studies (lab manual finalization, sample receipt documentation, handling, storage tracking, disposal, etc.).
  • Interact with Shipping and Receiving, Customs and Trade Compliance, Nonclinical Development, Global Clinical Operations, and SB bioanalytical groups.
  • Learn document and specimen archival processes, recalling or destruction of samples (including collaboration with the Document Management Associate).
  • Understand import/export requirements for biological samples (invoices, licenses, permits, declarative letters, etc.).
  • Use data transfer specifications to lead sample reconciliation efforts with study teams.
• Laboratory Operations
  • Assist with maintenance qualification processes and procedures for controlled temperature units.
  • Assist with testing new equipment or instruments.
• Quality Control
  • Learn good documentation practices and their importance in regulated work.
  • Learn procedures for reviewing work in regulated software (electronic lab notebook, plate readers, LIMS, etc.).
  • Perform other duties as assigned.

Qualifications

• Currently enrolled in a bachelor‚Äôs or Master‚Äôs program in pharmaceutical sciences, biomedical sciences, chemistry, biology, or a related field from an accredited college or university.
• Fundamental understanding and experience in a laboratory setting (course-related or previous internship).
• Strong organization, attention to detail, time management, and interpersonal skills.
• Interest in processes and procedures to ensure regulatory compliance.
• Working knowledge of Microsoft 365 suite.

Skills

• Communication and collaboration with cross-functional teams.
• Ability to learn and apply regulatory requirements (GLP, FDA).
• Process improvement mindset to enhance lab efficiency.

Education

• Not specified beyond required program enrollment (see Qualifications).

Additional Requirements

• Location: West Chester, PA. Length: minimum 12 weeks. Schedule: 40 hours/week onsite. Pay: TBD.