Intern-Quality Assurance (CLS)

Internship Details:

• Duration

: 20 weeks, full-time/Onsite •

: 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.

About Team:

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. •

• 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)

• 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 in Quality Assurance, Regulatory Compliance, Clinical Trial, or Bioanalytical Sciences.
• Strong English reading and writing skills; CET-6 or equivalent certification.
• Excellent communication and interpersonal skills, with a strong team-player mindset.
• Enthusiastic, self-confident, proactive, and driven by a strong desire to learn and grow.

• Good organization and multitasking ability.
• Able to communicate effectively with excellent verbal/written communication skills.
• Exceptional problem-solving and critical-thinking skills.
• Creative and self-motivated individuals who work collaboratively in a high-performance team environment.

As a Labcorp intern, you'll be immersed in hands-on work that complements your academic background. In addition to your project work, you'll gain valuable exposure to Labcorp's global business, culture, and leadership through:

• Enterprise-wide learning experiences

that introduce you to key business functions across Labcorp •