Quality Engineer

BD Nogales Norte; Plymouth; On-site; GBP 35,000 - 45,000; Full time

Job summary

A leading medical technology company is looking for an experienced Quality Engineer in Plymouth, UK. In this onsite role, you will oversee the quality system and enhance operational efficiency. Responsibilities include ensuring compliance with industry regulations, conducting investigations, and working with cross-functional teams. Ideal candidates will have a degree in Science or Engineering and experience in regulated environments. A salary of £35,000 to £45,000 is offered with benefits.

Qualifications

• Proven experience in a regulated environment (pharmaceutical, aerospace, or medical devices).
• Strong understanding of relevant regulations such as CFR Part 820.
• Demonstrated ability to develop and implement procedures and policies.

Responsibilities

• Ensure compliance with ISO13485 and other standards.
• Conduct product complaint investigations.
• Collaborate with cross-functional teams to improve operational efficiency.

Skills

Proficiency with MS Excel

Knowledge of ISO13485

Understanding of Quality Assurance principles

Excellent communication skills

Ability to manage multiple priorities

Education

Degree in Science or Engineering

Tools

Minitab

Job description

Job Description Summary

We have an exciting opportunity to recruit an experienced quality engineer to join our quality engineers within a 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.

Company Overview

BD is one of the largest global medical technology companies. Our purpose is to advance the world of health™ through imagination, passion, and transformative solutions.

Why Join Us

We are certified as a Top Employer 2025 in the United Kingdom, reflecting our commitment to an exceptional working environment. A career at BD includes learning, working alongside inspirational leaders, and shaping the trajectory of BD while leaving a legacy.

Main Responsibilities

• Ensure compliance with ISO13485, CFR Part 820, and other relevant regulations and standards.
• Monitor and maintain the quality system, ensuring continuous improvement.
• Conduct product complaint investigations and manage corrective actions 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.
• Utilise lean manufacturing techniques to reduce waste and improve operational efficiency.
• Identify and propose improvements to existing procedures.
• 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

£35,000 to £45,000 per year + benefits.

Location

GBR Plymouth – Belliver Industrial Estate (Primary work location). Remote or field‑based positions have different arrangements indicated in the job posting.

Employment Type

Full‑time.

Seniority Level

Mid‑Senior level.

Job Function

Quality Assurance. Industry: Manufacturing.

Equal‑Opportunity Employer Statement

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 status, familial status, sexual orientation, gender identity, genetics, disability, military eligibility or veteran status, or any other protected status.

How to Apply

Click on apply if this sounds like you! At BD, we prioritize onsite collaboration; most roles require a minimum of four days in‑office per week, with flexibility for remote or field‑based arrangements where applicable.