Regulatory Affairs Trainee

hace 4 semanas

Madrid, España BD A tiempo completo

**Job Description Summary**: As Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team. The activities are related with the execution of regulatory processes of products related with Surgery, Urology and Critical Care, and Peripheral Intervention business units as well as to support in projects where the team is leading or participating as the regulatory representative.

**We are the makers of possible**:
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

**Why join us?**:
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.

Become a **maker of possible** **with us

**Our vision for Regulatory Affairs at BD**:
The Regulatory Affairs team is helping to ensure speed to market for BD’s innovative medical technologies by having an acutely patient-centric mindset.

**About the role**:
**As** **Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team. The activities are related with the execution of regulatory processes of products related with Surgery, Urology and Critical Care, and Peripheral Intervention business units as well as to support in projects where the team is leading or participating as the regulatory representative.

**Main responsibilities will include**:

- Create, update and maintain databases and reports where regulatory information/documentation is kept
- Review and compile data packages to support regulatory submissions and customer queries across EMEA
- Develop and maintain communication tools to share RA updates across the EMEA region and facilitate collaboration with key stakeholders
- Assist in the preparation of regulatory procedures to ensure compliance with regulatory and corporate requirements
- Support the team with RA assessments for select projects, collaborating closely with global divisions, local affiliates and regional collaborators as needed

**About you**:

- University degree in Life or Engineering Science, Business, or equivalency
- Internship Agreement with the University is required.
- Excellent English

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

**Primary Work Location**: ESP San Agustin del Guadalix

**Additional Locations**:
**Work Shift**:

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