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
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
We are seeking a highly motivated Senior Regulatory Affairs Specialist to join our Quality, Regulatory Affairs (QRA) EMEA team. In this role, you will serve as a key regulatory expert supporting the Economic Operator (EO) Hub and ensuring compliance with evolving regulatory requirements across the European Union, United Kingdom, and Switzerland. You will play a critical role in monitoring regulatory developments, conducting impact assessments, and driving the implementation of compliance initiatives related to Authorised Representatives, Importers, and Distributors.
As a trusted subject matter expert, you will partner with cross-functional stakeholders to support regulatory operations, device registrations, technical documentation reviews, and economic operator activities. You will also contribute to the continuous improvement of quality system processes, support regulatory inspections and audits, manage interactions with Competent Authorities, and analyse compliance metrics to identify risks and improvement opportunities. This position offers the opportunity to influence regulatory strategy, strengthen compliance frameworks, and help ensure continued market access for medical devices across the EMEA region.
Main Responsabilities
Monitor regulatory developments across the EU, UK, and Switzerland, assessing their impact on Economic Operator activities and communicating requirements to relevant stakeholders.
Conduct regulatory impact assessments and gap analyses to evaluate compliance with new or updated regulations, guidance documents, and authority expectations.
Develop and execute compliance implementation plans, ensuring timely adoption of regulatory changes across the business.
Act as the regulatory subject matter expert for Economic Operator requirements, providing guidance and support to cross-functional teams and business partners.
Support key regulatory operations, including Authorised Representative activities, technical documentation reviews, and device registration processes.
Develop, maintain, and enhance quality system documentation, including procedures, work instructions, and compliance-related records.
Support internal and external audits, inspections, and regulatory assessments, providing regulatory expertise, documentation, and responses to compliance inquiries.
Analyse compliance metrics, manage regulatory databases, identify potential compliance risks, and deliver training and awareness programmes to promote a strong regulatory compliance culture.
About you
Strong knowledge of EU MDR (2017/745), IVDR (2017/746), UK Medical Device Regulations, and Swiss regulatory requirements, including Economic Operator obligations for Authorised Representatives, Importers, and Distributors.
Experience conducting regulatory impact assessments, gap analyses, and compliance evaluations, with the ability to translate regulatory changes into actionable implementation plans.
Hands-on experience supporting device registrations, technical documentation reviews, authorised representative activities, and regulatory submissions within the medical device industry.
Proficiency in quality management systems (QMS), including the development and maintenance of procedures, work instructions, CAPAs, audit support activities, and regulatory compliance documentation.
Strong analytical and project management skills, with experience using regulatory databases and compliance tracking systems to manage regulatory commitments, metrics, risk assessments, and continuous improvement initiatives.
This role it's a Fixed-Term Contract until February 2028
Salary Range €60K - €70K + Benefits
Click on apply if this sounds like you!
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
Optional Skills
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Primary Work Location
IRL Drogheda - Donore RdAdditional 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
€56,600.00 - €86,300.00 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