Intern-Quality Assurance (CLS)

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. Intern-Quality Assurance (Central Lab) Labcorp is seeking an Intern-Quality Assurance (Central Lab)  to join our team at  Shanghai, China. Internship Details: Duration : 20 weeks, full-time/Onsite Dates of Internship : Jan – May 2027 Compensation : Paid internship Eligibility : Final-year students who are expected to graduate in July 2027 are preferred. However, students at all academic levels who are pursuing relevant fields of study are encouraged to apply.

The Central Lab Quality Assurance Department provides independent oversight of clinical trial operations to ensure strict compliance with ISO 15189 standards, CAP, NMPA regulations, study protocols, and corporate quality procedures. Through rigorous inspections, audits, quality management system (QMS) oversight, and regulatory support, the department guarantees the integrity, reliability, and regulatory acceptance of clinical trial study data while driving continuous quality improvement across the organization. As a QA Intern, you will systematically immerse yourself in international medical laboratory standards, robust quality management systems, auditing methodologies, and evolving regulatory compliance frameworks. You will gain invaluable, hands-on experience in ISO 15189 accreditation preparation, sponsor audit assistance, and NMPA inspection highlights. Utilizing industry-leading platforms like the Veeva QMS, you will develop the analytical, communication, and problem-solving skills necessary to launch a successful career in the global pharmaceutical and clinical trial industries. Internship Assignment Summary: ISO 15189 Standards: Master the regulations, requirements, and accreditation processes for medical laboratories. Quality Management Systems (QMS): Gain practical experience in building and operating medical lab QMS. Regulatory Compliance: Stay ahead with deep insights into NMPA inspection priorities and mandate requirements. Audit & Inspection Management: Learn best practices for managing audits and inspections within the pharmaceutical sector. Veeva QMS: Acquire hands-on proficiency in navigating and operating the industry-leading Veeva quality management platform. Global Industry Exposure: Build a comprehensive understanding of international quality management frameworks across the pharma and clinical trial sectors. Mentorship & Collaboration: Work directly with elite quality and compliance teams to rapidly accelerate your professional capabilities and career trajectory.

Current enrollment in Biology, Biotechnology, Biochemistry, Pharmacy, Pharmaceutical Sciences, Chemistry, Life Sciences, Medical Laboratory Technology, and Immunology Bachelor's degree program. 3 months or more experience using computer and office software applications (e.g. Microsoft Word, Excel and Outlook) Preferred Qualifications: Highly responsible and detail-oriented with strong organizational and coordination skills. Possess foundational laboratory knowledge with a strong passion for pharmaceutical R&D, clinical research, or biotechnology industries. Interest