Intern-Quality Assurance (ED)

Posted 10 Hours Ago
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Shanghai, Shanghai Municipality, Shanghai, CHN
In-Office
Internship
Healthtech • Biotech
The Role
Supports the Preclinical GLP Quality Assurance team through document review, study and data audits, SOP lifecycle management, deviation and CAPA processes, data integrity oversight, regulatory inspection support, and quality system activities. The intern will develop knowledge of GLP regulations, auditing, compliance, risk-based quality oversight, and pharmaceutical and biotechnology research while collaborating with internal teams.
Summary Generated by Built In

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 (ED)

Labcorp is seeking an Intern-Quality Assurance (ED) 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.

About Team:

The Preclinical GLP Quality Assurance Department provides independent oversight of nonclinical studies to ensure compliance with GLP regulations, study protocols, and company procedures. Through inspections, audits, quality system oversight, and regulatory support, the department helps ensure the integrity, reliability, and regulatory acceptance of study data while promoting continuous quality improvement across the organization.

As a QA intern, you will learn GLP regulations, quality management systems, auditing techniques, data integrity principles, and regulatory compliance requirements. You will gain hands-on experience in document review, study audits, SOP management, deviation and CAPA processes, and inspection readiness activities, while developing analytical, communication, and problem-solving skills applicable to careers in pharmaceutical and biotechnology research.

Internship Assignment Summary:
  • GLP regulations and compliance requirements
  • Quality Management Systems (QMS)
  • Study, data, and report auditing
  • Data integrity and documentation practices
  • SOP lifecycle management
  • Deviation, investigation, and CAPA processes
  • Regulatory inspection support
  • Risk-based thinking and quality oversight
  • Professional communication and collaboration
  • Career pathways in QA, regulatory affairs, and drug development

Minimum Qualifications: 

  • Current enrollment in Pharmacy / Pharmaceutical Sciences, Toxicology, Veterinary, Chemistry Bachelor's degree program.
  • 3 months or more experience using computer and office software applications (e.g. Microsoft Word, Excel and Outlook)

Preferred Qualifications:

  • Good written and reading proficiency in English; CET-4/6.
  • Strong spoken English skills.
  • Interest in Quality Assurance, Regulatory Compliance, Clinical Research, or Bioanalytical Sciences.
  • Coursework or laboratory experience related to biotechnology, pharmaceutical sciences, analytical chemistry, or biologics.
  • Exposure to GCP, GLP, or other regulated laboratory environments through coursework, training, or internship experience.
  • Familiarity with data management systems or quality management processes.
  • Experience with scientific data analysis.

Additional Job Standards:

  • 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.

About the Program 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
  • Leadership exposure and visibility, including direct interaction with senior leaders
  • An immersive, in-person Workshops designed to connect you with peers and deepen your understanding of our mission
  • Senior leader speaker sessions offering insights into strategy, innovation, and career growth
  • Continuous opportunities to connect and grow, from intern cohort communication channels and LinkedIn Learning resources to professional development sessions and storytelling opportunities that highlight your internship journey
  • Connection to Labcorp’s inclusive culture through engagement with our employee resource groups (ERGs)and values-driven community initiatives
  • Dedicated mentoring connections to guide your growth, provide career advice, and support your internship journey

Apply now to launch your career and create real impact for patients worldwide. #FutureofLabcorp

At Labcorp we have a passion for helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step!


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 


We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.


Skills Required

  • Currently enrolled in a Bachelor's degree program in Pharmacy, Pharmaceutical Sciences, Toxicology, Veterinary Science, or Chemistry
  • At least 3 months of experience using computer and office software applications, such as Microsoft Word, Excel, and Outlook
  • Good written and reading proficiency in English; CET-4/6
  • Strong spoken English skills
  • Interest in Quality Assurance, Regulatory Compliance, Clinical Research, or Bioanalytical Sciences
  • Coursework or laboratory experience in biotechnology, pharmaceutical sciences, analytical chemistry, or biologics
  • Exposure to GCP, GLP, or other regulated laboratory environments through coursework, training, or internship experience
  • Familiarity with data management systems or quality management processes
  • Experience with scientific data analysis
  • Good organization and multitasking ability
  • Effective verbal and written communication skills
  • Strong problem-solving and critical-thinking skills
  • Ability to work collaboratively in a high-performance team environment
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The Company
HQ: Burlington, NC
19,796 Employees
Year Founded: 1978

What We Do

We believe in harnessing science for human good. And so we work day and night, around the world, to deliver answers for all your health questions—whether you’re a provider, drug developer, hospital, medical researcher or patient. That means everything from advancing diagnostic testing to helping launch new drugs, to offering new perspectives through data - all drawing from a deep well of scientific expertise. So when you need trusted information to make clear, confident health decisions, consider us your source.

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