Job Description Summary

Are you Quality driven? Are you passionate about the medical industry? Then, this is the job you are looking for! At BD, we are looking for someone to join our EDC Quality Team in Temse.

As a Quality Engineer, you are responsible for managing EMEA quality processes and controls associated with CAPA management and Audits as well as possible other activities related to European regulations and ISO compliance, corporate directives and company strategies (such as document control, change management, validation activities ...).

Job Description

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!

Your Responsibilities

• Maintain and improve the Quality Management System through internal  document revision, quality training, and process improvement initiatives.
• Works closely with other departments to ensure compliance and maintain the highest quality standards.
• Responsible for the follow-up on non-conformances, CAPA's, change controls, validation, quality metrics ....
• Ensure that the audits are performed as per the audit plan and make sure all auditors follow the required training.

Your Profile

• You have a Master or a Bachelor degree.
• You have experience in ISO and European Regulations, preferably medical device industry, with exposure to document and data control processes.
• You are able to work within a Quality Management System especially ISO9001 an ISO 13485.
• You have the ability to influence others and move toward a common vision or goal.
• You are able to work effectively at all levels in an organization.
• You are fluent in Dutch and English.
• Experience in validation is a plus
• Experience in GDP/GMP regulation is a plus

What we can offer you:

• A varied function with international contacts, within a company with an important social contribution in a value-driven organization.
• An informal working atmosphere, dynamic corporate culture, and an environment that lets you grow and develop.
• Unlimited possibilities for further development of your career, nationally and internationally.
• An attractive remuneration package.

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

Primary Work Location

BEL Temse - Laagstraat

Additional Locations

Work Shift