Job Description Summary

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!

This is a night shift position. Working hours are 11pm - 11am.

3 days on 3 days off.

Responsibilities:

• Raising Quality Notifications in accordance with standardized practices and ensuring that the non-conforming product is segregated and identified in accordance with the relevant procedures.

• Device History Record auditing to ensure that all records are complete and comply with GMP requirements.

• Product inspections as required by the process control plans which may include moulding product dimensional checks, functional checks and any others that require Quality support. 

• Support of Validation / trial runs in manufacturing ensuring product is controlled appropriately.

• Provide support for internal audits, third party regulatory audits and customer complaints as required.

• Providing a source of advice / knowledge on shift to manufacturing / technical associates on all matters relating to Quality.

• Supporting the Quality Engineering team on reasonable requests as they may arise. Conducting regular cycle counts of hold work as required. Supporting operational CI initiatives as required including documentation improvements.

Preferred requirements:

• Ideally GCSE Maths and English qualifications.

• Experience in a quality role within a high volume medical device-manufacturing controlled environment. 

• Basic knowledge of Six Sigma and Lean Manufacturing principles.

• Good numeracy and literacy skills.

• Working knowledge of MS Office and Minitab.

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

Required Skills

Optional Skills

.

Primary Work Location

Additional Locations

Work Shift