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:

• Represents quality interests and concerns on project teams.

• Leads risk management activities and leads the Quality engineering activities for NPI projects.

• Must be able to handle multiple projects and tasks, from product inception through product launch and maintenance.

• Develops or assists in development of inspection and test methods per product specifications.

• Performs test method validations and component qualifications as required

• Performs DOE’s and other statistical analysis to support product and process optimization or determine causes of process variation.

• Identifies quality systems engineering improvement opportunities and executes through the change management system

• Participates in internal audit and supplier audit programmes

• Participates on teams responsible for investigating and providing corrective action for production and supplier nonconformances.

• Develops robust action plans, projects and verification activities for elimination of potential at compliance and CAPA related risks, as required

• Assists in the Company’s complaint and failure investigation process.

About you

• You will be technically qualified with a bachelor’s degree, preferably in an Engineering, Technical or Science discipline.

• 5 years’ experience in the Medical Device or Pharmaceutical industry.

• Knowledge of quality management systems ISO 13485, GMP etc.

• Experience with combination products is an advantage.

• Excellent interpersonal skills with the ability to work in a team environment and work under own initiative to targets and deadlines coupled together with problem solving techniques with excellent organisational skills.

• Dedication to excellence, flexibility and adaptability to change are also a plus.

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