Internship in Regulatory Affairs
Purpose of the role
We are looking for two creative, innovative and open-minded interns 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 Roche Diagnostics' vision: innovating diagnostics, shaping healthcare & changing lives.
Your key responsibilities
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 you are
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.
What do we offer?
Become a Regulatory Affairs professional for IVDs.
Develop a Regulatory Mindset and understand the most important regulations and industry standards.
Obtain a unique view of end-to-end IVD development and other functions involved.
Exposure to other functions and networks within the organization.
Gain experience in a fast-paced, technological and international environment.
Lots of learning and a great team to mentor and guide you.
The preferred start date of the internship is July 2023 or upon availability. The duration of the internship is 12 months.
Please clearly indicate your preferred starting date of internship on your motivation letter.
Who we are
At Roche, 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.
Roche is an Equal Opportunity Employer.
