Job Description

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 - @EmmesCROFind us on LinkedIn - Emmes