Job Description Summary : 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!
About the role The Project Quality Engineer (PQE) is responsible for the implementation and/or modification of processes/products, supporting production to improve processes through continuous improvement, process analysis, six sigma analysis and validation.
Main responsibilities will include: Plan and deploy the Global Quality Requirements at plant level.
Ensure that the processes and products in their scope are aligned with the Plant Quality Systems.
Participate in the validation of each product in their scope and other processes.
Define control plan (In Process Control, Final Inspection) in production based on BD requirements.
Review and analyze quality data trends.
Lead the development of validation strategies and ensure their progress.
Follow up and resolution of non-conformances.
Project transfer activities.
Implement and ensure the data integrity of manufacturing processes.
Lead the CAPA process and ensure issue resolution.
Lead improvement projects.
Train the local operational team on product trainings.
About you Academic Background: - Engineering degree Valuable Complementary Training: Master's degree in Quality Management or Science.
Knowledge of Process Validation, Design Control, and experience in FMEA/Risk Management.
Understanding of industry regulations / standards: ISO13485, GMP, 21CFR820.
Microsoft Visio and Project.
Languages: - Fluent English Previous Experience: - Minimum experience of 3 years in a Quality Engineer role in industrial environments.
- Validations in a regulated industry (Healthcare / Pharmaceutical / Biologics / Medical Devices).
- Project management.
- ISO Management Systems and system/process audits (internal and external).
- Standardized continuous improvement methodologies (PDCA, 8Ds, Lean tools).
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.
Primary Work Location : ESP Zaragoza #J-18808-Ljbffr