INTERNSHIP DETAILS

Quality Assurance Intern

CompanyEmmes Global
LocationIndia
Work ModeOn Site
PostedJanuary 7, 2026
Internship Information
Core Responsibilities
Interns will contribute to quality operations, including change management and quality incident management. They will also support regulatory inspection readiness activities and develop tools for reporting quality assurance metrics.
Internship Type
full time
Company Size
1243
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
For over 40 years, our team of 1,000+ experienced professionals have provided the full range of Contract Research Organization expertise necessary to conduct clinical research with a firm scientific basis that is fully compliant with national and international regulatory guidelines. With offices throughout the US, Europe, Canada, and India, Emmes supports the advancement of global public health and biopharmaceutical innovation through disciplined science, rigorous research, fact-based decision-making, and operational excellence. Emmes possesses knowledge across a broad range of therapeutic areas, with specializations in Vaccines and Infectious Diseases, Ophthalmology, Immunology and Neuroscience. From comprehensive support of pandemic research to groundbreaking work in cell and gene therapy across the globe, Emmes has collaborated on clinical research across a wide array of disease states in over 75 nations. As a strategic collaborator with applied talent in over 2,000 clinical trials and contributions to over 2,500 publications that advance the understanding of medicine and public health, Emmes is committed to expanding the services offered to best meet the changing needs of clients and studies. Ongoing investments in global clinical research capabilities, innovative data management platforms, biostatistics/bioinformatics expertise, and people have enabled Emmes to provide a multi-faceted approach to help you meet your research objectives. Emmes is a diverse, inclusive, innovative CRO that values integrity, agility, passion for excellence, collaborative partnerships, and intellectual curiosity.
About the Role
Overview

 

 

Emmes Group: Building a better future for us all.

 

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

 

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

 

Primary Purpose

 

We are looking for enthusiastic and motivated Quality Assurance Interns with strong aptitude, analytical thinking, logical reasoning, and attention to detail. As an intern, you will work alongside our corporate and clinical quality assurance team, gaining hands-on experience with clinical quality and general quality management system activities.


Responsibilities

  • Contribute to quality operations such as change management, quality incident management (CAPA), and controlled documents management.
  • Review documents for accuracy and compliance
  • Apply analytical and logical thinking to optimize processes and create efficiencies.
  • Support regulatory inspection readiness activities and audit teams
  • Develop tools for reporting of quality assurance metrics

What You'll Gain

  • Knowledge and skills pertaining to quality operations at a global CRO
  • Opportunity to apply technical skills that will streamline processes and increase operational efficiency.
  • Mentorship from experienced quality assurance professionals.
  • Potential to transition into a full-time role based on performance.

Qualifications

 

  • Life Sciences Master’s degree
  • Contribute to quality operations such as change management, quality incident management (CAPA), and controlled documents management.
  • Review documents for accuracy and compliance
  • Apply analytical and logical thinking to optimize processes and create efficiencies.
  • Support regulatory inspection readiness activities and audit teams
  • Develop tools for reporting of quality assurance metrics

CONNECT WITH US!

Follow us on Twitter - @EmmesCRO

Find us on LinkedIn - Emmes

 

Key Skills
Quality AssuranceAnalytical ThinkingAttention To DetailChange ManagementQuality Incident ManagementControlled Documents ManagementRegulatory Inspection ReadinessAudit SupportProcess OptimizationEfficiency CreationQuality Assurance MetricsDocument ReviewCollaborationClinical ResearchTechnical SkillsMentorship
Categories
HealthcareScience & ResearchAdministrative