Job ID R-552960 Date posted 08/13/2026

Be part of something bigger at BD. Here, you’ll help us maintain our high standards from a regulatory perspective at all levels, with a keen focus on submissions. It requires acute attention to detail, excellent communication skills and a passion to keep learning and updating your knowledge, which we’ll help you do with regular learning opportunities. Here, you’ll use your in-depth knowledge of FDA, Canadian and ISO/MDD regulations and requirements surrounding medical devices to ultimately achieve a singular goal: advancing the world of health™. At BD, you can make a true difference of one.

  • Job Type:
    Full-Time
  • Job Level:
    Entry to Senior
  • Travel:
    Varies
  • Salary:
    Competitive
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Responsibilities

We are the people who give possibilities purpose

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.

Job Description

Join BD's Specimen Management Regulatory Affairs team and gain hands-on experience in supporting regulatory activities across the EMEA region. This trainee opportunity offers exposure to medical device and in vitro diagnostics regulations while contributing to a key business initiative: the Technical Data Sheet (TDS) Automation Project. You will collaborate with cross-functional teams, support regulatory documentation processes, and help ensure compliance of product information used in customer tenders and business operations.

Responsibilities

  • Support the Regulatory Affairs team in activities related to the Technical Data Sheet (TDS) Automation Project.

  • Review and verify regulatory information extracted from approved and validated sources for inclusion in TDS documents.

  • Assist the Specimen Management business during the transition from the legacy TDS platform to the new automated system.

  • Support the review of advertising and promotional materials to ensure compliance with applicable regulations and company procedures.

  • Maintain regulatory documentation, repositories, and product-related records with a high degree of accuracy.

  • Provide administrative and regulatory support to cross-functional stakeholders and contribute to ongoing Regulatory Affairs projects.

Preferred Requirements

  • Bachelor's degree in Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field. Master's degree is an advantage.

  • Understanding of medical device and/or in vitro diagnostic regulatory frameworks.

  • Strong written and verbal communication skills with the ability to work effectively across teams.

  • Excellent attention to detail and documentation management capabilities.

  • Strong organizational skills with the ability to prioritize multiple tasks and deadlines.

  • Fluent in English, both written and spoken. Additional European languages are a plus.

What We Offer

  • A unique opportunity to gain practical Regulatory Affairs experience within a global MedTech leader.

  • Exposure to international regulatory processes and cross-functional collaboration.

  • Development opportunities through coaching, training, and participation in key business projects.

  • A dynamic and supportive work environment focused on learning and professional growth.

Internship allowance (ayuda estudio) - EUR 950/month (gross)

Why Join Us?

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 healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to 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, and other legally protected characteristics.

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Primary Work Location

ESP San Agustin del Guadalix

Additional Locations

Work Shift

At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

Salary Range Information

€20,200.00 - €30,775.00 EUR Annual
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Success Profile

What makes a successful Regulatory Affairs Professional at BD? Check out the top traits we’re looking for and see if you have the right mix.

  • Analytical
  • Collaborative
  • Communicator
  • Persuasive
  • Problem-solver
  • Skilled presenter

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