Ofertes d'ocupació per a Educació i Formació a Sant Cugat del Vallès

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• Tipus de contracteA temps complert
• Publicada8 de juny

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

Graduate Intern - Regulatory Affairs

We advance science so that we all have more time with the people we love.

Department Summary

We are looking for 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.

The Opportunity

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
  
  

• Intensive 1 year intern graduate program (Contrato en practicas)
• Competitive salary and benefits package
• Program start dates are in September
• Location in Sant Cugat del Valles, On site
• Access to training and development opportunities
• Work with some of the most talented people in the biotechnology industry
  
  
  

• You have recently graduated (within the last 3 years)
• 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)