Quality Engineer

Join to apply for the Quality Engineer role at BD Job Description Summary We have an exciting new opportunity to recruit an experienced quality engineer to join our quality engineers within the plant of 800+ employees. In this onsite role, 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. About BD 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? BD is proud to be certified as a Top Employer 2025 in United Kingdom, reflecting our commitment to creating an exceptional working environment. 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. Main 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. About You 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. Salary range for the role: £35,000 to £45,000 + benefits Click to apply if this sounds like you At BD, we prioritize on‑site collaboration because we believe it fosters creativity, innovation, and effective problem‑solving, which are essential in the fast‑paced healthcare industry. For most roles, we require a minimum of 4 days of in‑office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognising the importance of flexibility and work‑life balance. Remote or field‑based positions will have different workplace arrangements which will be indicated in the job posting. 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 #J-18808-Ljbffr