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Regulatory Affairs Specialist
full-timeGrenoble, San Agustín del Guadalix$36k - $58k

Summary

Location

Grenoble, San Agustín del Guadalix

Salary

$36k - $58k (EUR)

Type

full-time

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About this role

Job Description Summary

Being a key strategic partner for the EMEA BD Business by (i) supporting the implementation of registration/regulatory strategies for the UCC-SRG portfolios, closely aligned with the region's commercial objectives, to meet EMEA market requirements and (ii) securing local markets by maintaining local licenses compliant with changes related to local/global regulations or changes to the product(s).

Job Description

Responsibilities:

  • Drive alignment between regional regulatory strategies and Business Unit and Country RA objectives within BD’s matrix organization.

  • Prepare and compile registration and/or notification dossiers in collaboration with BU and Country RA teams to support timely submissions and renewals.

  • Lead registration planning and prioritization activities in EMEA to ensure strong alignment with business goals.

  • Execute product launch plans, renewals, and amendments, ensuring adherence to regulatory requirements and approved eIPPRA submissions.

  • Conduct impact assessments for product and regulatory changes within EMEA to ensure continued compliance for medical devices and pharmaceutical products.

  • Maintain Regulatory Information Management (RIM) systems, internal registration databases, and tracking tools to ensure data accuracy and transparency.

Preferred Requirements:

  • Scientific educational background preferred.

  • 5–10 years of Regulatory Affairs experience, ideally across both Pharmaceutical and Medical Device sectors, with international exposure.

  • Strong organizational, planning, and prioritization skills with the ability to manage multiple tasks.

  • Excellent verbal and written communication skills, with the ability to work cross‑functionally and across cultures.

  • High attention to detail with a focus on accuracy and completeness in all regulatory deliverables.

  • Fluent, native‑level English proficiency; computer‑literate and comfortable working in an international environment.

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!

Click on apply if this sounds like you!

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

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.

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

Required Skills

Optional Skills

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Primary Work Location

FRA Grenoble

Additional Locations

ESP Barcelona, ESP San Agustin del Guadalix

Work Shift

At BD, we are strongly committed to investing in our associates—their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You.

Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates’ progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. 

The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.

Salary Range Information

€36,400.00 - €58,225.00 EUR Annual

Other facts

Tech stack
Regulatory Affairs,Registration Strategies,Medical Devices,Pharmaceuticals,Impact Assessments,Data Accuracy,Communication Skills,Organizational Skills,Planning Skills,Prioritization Skills,Cross-Functional Collaboration,Attention to Detail,Scientific Background,International Exposure,Regulatory Compliance,Regulatory Information Management

About BD

BD is one of the world's largest medical technology companies that produce and sell medical equipment, medical systems and reagents, dedicated to improving human health around the world.
BD focuses on improving drug treatment, improving the quality and speed of diagnosis of infectious diseases, and promoting the research and discovery of new drugs and vaccines.
BD has strong research and development capabilities to fight many of the world's most intractable diseases.
Founded in New York in 1897, the company is headquartered in Franklin Lake, New Jersey, USA and employs more than 25000 people in about 50 countries around the world.
The company's clients include medical institutions, life sciences research institutes, clinical laboratories, industrial units and the general public.

Team size: 501-1,000 employees
Industry: Medical Equipment Manufacturing

What you'll do

  • The Regulatory Affairs Specialist will support the implementation of registration and regulatory strategies for the UCC-SRG portfolios, ensuring alignment with commercial objectives. They will also maintain local licenses compliant with regulatory changes and lead registration planning activities in EMEA.

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Frequently Asked Questions

What does BD pay for a Regulatory Affairs Specialist?

BD offers a competitive compensation package for the Regulatory Affairs Specialist role. The salary range is EUR 36k - 58k per year. Apply through Clera to learn more about the full compensation details.

What does a Regulatory Affairs Specialist do at BD?

As a Regulatory Affairs Specialist at BD, you will: the Regulatory Affairs Specialist will support the implementation of registration and regulatory strategies for the UCC-SRG portfolios, ensuring alignment with commercial objectives. They will also maintain local licenses compliant with regulatory changes and lead registration planning activities in EMEA..

Why join BD as a Regulatory Affairs Specialist?

BD is a leading Medical Equipment Manufacturing company. The Regulatory Affairs Specialist role offers competitive compensation.

Is the Regulatory Affairs Specialist position at BD remote?

The Regulatory Affairs Specialist position at BD is based in Grenoble, Auvergne-Rhone-Alpes, France and San Agustín del Guadalix, Madrid Community, Spain. Contact the company through Clera for specific work arrangement details.

How do I apply for the Regulatory Affairs Specialist position at BD?

You can apply for the Regulatory Affairs Specialist position at BD directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process.