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.
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Job Type:
Full-Time -
Job Level:
Entry to Senior -
Travel:
Varies -
Salary:
Competitive -
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
As a Senior Regulatory Affairs Specialist, you will provide regulatory expertise across BD's infusion preparation and delivery (IPD) portfolio, including disposable infusion sets and accessories used for the administration of fluids and medications. The Sr. Regulatory Affairs position will report to the Sr. Manager, Regulatory Affairs and will be based at the Sendal Almaraz facility in Spain.
The successful candidate will support a global regulatory affairs team through a variety of registration activities that may span new product development, design changes, sustaining engineering, and market access initiatives for Class I and II/IIa devices.
Working closely with Quality, Research & Development, Medical Affairs, Marketing, and other key stakeholders, the candidate will ensure that regulatory requirements are effectively integrated into project planning, execution, and technical documentation, enabling product compliance, global market access, and successful commercialization.
Main responsabilities will include:
Support product development and change control projects byidentifyingand interpreting applicable regulatory requirements,providingregulatory guidance throughout the project lifecycle, and reviewing and approving project documentation (e.g., design verification reports, technical documentation, labeling) to support regulatory submissions and compliance activities.
Contribute to first-to-market commercialization opportunities by deliveringtimelyregulatory support and strategies thatfacilitateefficient product launches and market access.
Collaborate cross-functionally with Quality, Research & Development, Medical Affairs, Marketing, and other key stakeholders to ensure regulatory requirements are effectively integrated into project deliverables and technical documentation.
Prepare,maintain, and update technical documentation, regulatory submissions, and product registrations to support market access and continued compliance in global markets.
Interpret, assess, and communicate applicable regulatory requirements, standards, and guidance documents (e.g., EU MDR, FDA, ISO standards, and international regulations) to cross-functional teams in a clear and actionable manner.
Qualifications
Bachelor's degree in Regulatory Science, Biomedical Engineering, Pharmaceutical Sciences, Life Sciences, or a related scientific discipline
Approximately3-5years of experience in Regulatory Affairswithin themedical deviceindustry.
Strong knowledge of medical device regulatory requirements and processes, with experience supporting regulatory submissions, product registrations, technical documentation, or compliance activities.
Understanding of Regulation (EU) 2017/745 (EU MDR), UK MDR, U.S. FDA requirements, and/or other international regulatory frameworks.
Experience working within a regulated environment andISO 13485Quality Management System
Experience contributing to technical documentation, change control activities, product development projects, or sustaining engineering initiatives.
Strong analytical and problem-solving skills, with the ability to interpret regulatory requirements and apply them to practical business situations.
Ability to manage multiple priorities effectively whilemaintaininga high levelof accuracy and attention to detail.
Strong written and verbal communication skills, with the ability to collaborate effectively across cross-functional teamsto build effective working relationships.
Develop,maintain, and continuously improve regulatory procedures and processes to ensure ongoing compliance with applicable regulatory and quality management system requirements.
Proactivelyidentifyregulatory risks, issues, and project roadblocks; analyze data todetermineroot causes and effectively communicate recommendations and mitigation strategies to project teams and management.
Provide regulatory support for customer inquiries, product information requests, tender submissions, and other commercial activities asrequired.
Supportcontinuous improvement initiatives within Regulatory Affairs, Quality Management Systems, and broader business processes to enhance compliance, efficiency, and organizational effectiveness.
Salary range for this role: EUR 37,700.
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.
Required Skills
Global Regulatory, Medical Device Regulations, Product Registrations, Regulatory SupportOptional Skills
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Primary Work Location
ESP Almaraz - Ctra. NacionalAdditional 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
€37,700.00 - €60,350.00 EUR AnnualSuccess 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