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!

Main responsibilities will include:

• Quality Assurance: Manages and improves a quality system in accordance to BDX guidelines and standards, and compliant with local governmental regulations on a national scale which apply to BDX country activities, business needs and internationally marketed products and services
• Manage and maintain certification of ISO 13485 requirements across the go to market entity for the Benelux
• Supplier performance: Ensure that suppliers with a quality impact used by the organization are selected, classified, evaluated, and monitored and that records of this assessment are maintained.
• Management Review: Coordinate periodically meetings and prepare and submit quarterly management reports relating to company systems, compliance, and incidents. Ensure that the performance of the QMS is reviewed at planned intervals to ensure its continuing suitability, adequacy, and effectiveness.
• Manage any local inspections & audits and ensure appropriate engagement with local, regional and business leadership
• NCR & CAPA management: Co-ordinate continual improvements of the QMS, ensuring that evidence of corrective and preventive actions taken are recorded and reviewed.
• Training: Maintain the QMS training plan for Benelux. Ensure that all new staff are inducted into the requirements of the QMS related to their own roles and responsibilities. Provide refreshment training as necessary

About you

• Proven experience working ideally in a medical device/pharma/pharmacy environment
• ISO 13485 knowledge
• Strong relationship building skills; demonstrated leadership coupled with the ability to work well with people at all levels and in all functions of the organization as well as with external regulatory agencies.
• Good analytical skills; attention to detail and ability to manage multiple tasks and priorities at the same time.
• Excellent communications, technical and presentation skills.
• Computer skills (Advanced with Microsoft Excel, Word, Outlook and PowerPoint)
• Language skills: Dutch and English essential and French preferred.

Click on apply if this sounds like you!

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