BD
Quality Engineer (Part-Time)
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Job Description
Company Overview
We are the people who give possibilities purpose. 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.
Role Overview
We have an exciting new opportunity to recruit an experienced quality engineer to join our quality engineers within the plant of 800+ employees. As a Quality Engineer, you will oversee all operational aspects of the quality system, enhance operational efficiency on the manufacturing floor, manage non-conforming materials, and drive continuous improvement through effective change management. This is a part-time position.
In our Quality team, we collaborate on a large scale, focusing on making sure everything is correct, effective, and efficient to bring the highest-quality and most competitive products and services to our customers and their patients.
Responsibilities
- Ensure compliance with relevant regulations and standards, including ISO13485 and CFR Part 820.
- Monitor and maintain the quality system, ensuring continuous improvement.
- Conduct product complaint investigations and manage corrective actions, from implementation to closure.
- Develop, implement, and monitor procedures and policies to ensure adherence to standards.
- Collaborate with cross-functional teams such as Manufacturing, Engineering, and Supply Chain to achieve organisational performance goals.
- Utilise lean manufacturing techniques to reduce waste and improve operational efficiency.
- Identify and propose improvements to existing procedures to enhance efficiency.
- Participate in cross-functional teams to drive project success.
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Preferred Requirements
- Ideally, a Degree in Science or Engineering discipline.
- Proven experience in a regulated environment, ideally within the pharmaceutical, aerospace, or medical device manufacturing industries.
- Demonstrated knowledge of ISO13485, CFR Part 820, or equivalent regulations and standards.
- Strong understanding of Quality Assurance principles and methodologies in a regulated setting.
- Proficiency with MS Excel, Minitab, or similar statistical analysis tools.
- Excellent written and verbal communication skills.
- Ability to work effectively as part of a team and manage multiple priorities simultaneously.
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Salary Range
£14,000 - £27,000 + benefits
Why Join Us?
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 healthcare. At BD, you’ll discover a culture in which you can learn, grow, and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
Primary Work Location
GBR Plymouth - Belliver Industrial Estate
Salary Range Information
£33,300.00 - £50,775.00 GBP Annual
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to 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, and other legally protected characteristics.
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