Quality Engineer

BD

As the Quality Engineer, you will support manufacturing of peripheral interventional devices. This role will represent quality interests and concerns on day to day quality operations to ensure conforming materials are available for manufacturing and customers.

You will work with different function across the business on problem solving and investigations to determine root cause of material non-conformances so that issues are resolved to close out with no recurrences.

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!

Our vision for Peripheral Intervention at BD

Our Peripheral Intervention (PI) business unit offers a comprehensive range of medical products, devices and services for the treatment of peripheral arterial and venous disease, cancer detection, and end-stage renal disease and maintenance.

This role is offered on a 12 month FTC basis.

Main responsibilities will include:

  • Ensure compliance to quality system requirements as defined by procedures, FDA QSR, ISO 13485 and applicable international and national standards (e.g. EN, ASTM) through active participation in the divisional and cross divisional product and process development system
  • Perform timely disposition of non-conforming materials from incoming Quality Control or Manufacturing Processes, to ensure continued material compliance
  • Provides technical support on components, material methods, systems, equipment & process optimisation
  • Support continuous improvement initiatives related to quality process to drive performance and compliance
  • Support cost savings projects including scrap reduction (Quality improvements), uptime improvement and process simplification to reduce risk
  • Apply Quality Engineering tools (Sampling Plans, Root Cause Analysis, Statistics, etc.)
  • Apply and improve procedures for consistent and effective implementation of Quality System
  • Review documentation to ensure accuracy and compliance to procedures and regulations
  • Develop or assist in development of inspection and test methods per product specifications
  • Perform test method validations as required
  • Support internal and external supplier audits
  • Identify quality systems engineering improvement opportunities and executes through the change management system

About you:

  • Bachelor degree in one of the following fields: Mechanical, Biomedical, Chemical or other related engineering discipline or Technical/Science qualification (level 8).
  • 2+ years of industrial experience in quality engineering or similar, preferably in medical device or other regulated FDA/QSR and ISO environment.
  • Experience in Risk Management process (PFMEA is preferred)
  • Excellent attention to detail and adaptability
  • Excellent interpersonal skills with the ability to work in a team environment and work under own initiative to targets and deadlines
  • Problem solving techniques with excellent organisational skills
  • Excellent oral and written communication skills.
  • Ability to analyse data, interpret results, and write reports.
  • Experience in process validation (IQ, OQ and PQ) is a plus.
  • Proficient in statistic software is 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.

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