Intern in Regulatory Affairs

Job Description:

(COMPANY NAME) fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people's varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join (COMPANY NAME), where every voice matters.

The Position

Intern in Regulatory Affairs

Purpose of the role

We are looking for a creative, innovative and open-minded intern to join the Global Regulatory Affairs team.
As an Intern in Regulatory Affairs, you have the opportunity to support regulatory and product care activities, and get insights into the IVD industry and the applicable regulations and standards for IVD products.
In Global Regulatory Affairs we work on specific challenges as a team within all areas of the diagnostic business around the globe, to grow together to bring the best products to patients while choosing a work environment that fits our life.
In this role, you can demonstrate your creativity and leave a footprint in our products' lifecycle. Here you will directly contribute to (COMPANY NAME) Diagnostics' vision: innovating diagnostics, shaping healthcare & changing lives.

How would your day to day look like?

After your ramp-up, you will be assigned to tasks or projects. You'll be mostly spending your time in:
* You assist in the worldwide registrations and activities for various IVD products, at various stages of their development and lifecycle
* You support the preparation and maintenance of global documentation for our IVD products
* You collaborate with other regulatory affairs teams, including local affiliates, for registrational activities
* You coordinate with global interdisciplinary project teams to provide regulatory input to development, submission planning, and documentation needed
* You support the global regulatory team members in their non-registrational activities

Who are you?

You have recently graduated (within the last 3 years) in the field of Life Sciences, Biology, Chemistry or Engineering
* You possess facilitation and communications skills and the ability to deal with adversity in a multicultural and international environment
* You are a fast learner, have a proactive attitude to drive solutions, and have a high level of team orientation
* You are curious and attentive to detail
* You are fluent in English (written and spoken)
If you already have previous experiences in the field of Medical Devices and/or basic knowledge of regulations, this is a plus.

This opportunity is part of the START TECH program, you can find more information about the program in the following link:
https://careers.(COMPANY NAME).com/global/en/start-tech-program-spain

Who we are

At (COMPANY NAME), more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we've become one of the world's leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

(COMPANY NAME) is an Equal Opportunity Employer