Quality Systems Engineer

Skip to main contentJobsDashboardProfileJoin Talent NetworkSign InEnglishSingle PositionENGAGE. INSPIRE. DEVELOP.View All JobsQuality Systems EngineerLivingston, United KingdomApply NowAdd to Job CartFind out how well you match with this jobUpload your resumeJob descriptionCompany blogJob IDR039661About usAt Plexus, our vision is to help create the products that build a better world.  By embracing an innovative culture of excellence, we pride ourselves on designing, manufacturing and servicing some of the world’s most transformative products. From life-saving medical technology and mission-critical defense solutions to sophisticated industrial automation, we’re proud to partner with our customers to bring their complex ideas to market. Visit Plexus.com to learn more about our unwavering commitment to our vision. Living Our ValuesWith a vision rooted in the wellbeing and inclusive engagement of our team members, our customers, their end users and our communities, people are the heart of what we do and who we are. Our values unite and guide us in everything that we do. Our values include: Growing our People, Building Belonging, Innovating Responsibly, Delivering Excellence and Creating Customer Success. As part of our team, you’ll do impactful work within an inclusive environment where everyone works together to achieve extraordinary outcomes. You’ll be empowered to reach your full potential through managing your own personalised development plan and access to our learning and development programs.The RoleWe are seeking a Quality Systems Engineer to championed compliance and drive continual improvement across our Quality Management Systems (QMS). In this role, you will be a key player in maintaining our high standards, navigating diverse regulatory landscapes, and ensuring our processes are robust and future-proof.Key ResponsibilitiesAudit Leadership: Lead, manage, and participate in internal and external audits (including customer visits, regulatory inspections, and registrar/certification audits). You will also oversee the creation and maintenance of our internal audit schedule.CAPA Management: Support and coordinate Corrective and Preventive Actions (CAPA) to ensure swift resolution, robust follow-through, and transparent reporting to leadership.Continuous Improvement & Special Projects: Drive QMS enhancements by assisting with process validations and critical documentation (e.g., assembly build instructions, device travelers, certificates of compliance, DMRs, and DHRs).Regulatory Compliance: Stay ahead of ever-changing industry standards and regulatory requirements. You will help establish regulatory guidelines across various market sectors and collaborate with site quality managers to ensure regional compliance.Standard Mastery: Work closely with frameworks such as ISO 9001, ISO 13485, AS 9100, Nadcap, and ISO 14001.Cross-Functional Communication: Support the design and implementation of the quality system while effectively communicating regulatory requirements to internal stakeholders.What We Are Looking ForEducation & Experience:Preferred: A Bachelor’s degree with 2+ years of related experience.Equally Valued: We welcome applications from candidates with an equivalent, proven combination of education and hands-on industry experience.Core Skills:Mindset: Self-motivated, proactive, and equally comfortable working independently or collaborating in a team environment.Communication: Strong oral and written communication skills with the ability to translate complex regulatory requirements into actionable steps.Technical Aptitude: Excellent problem-solving abilities, sharp attention to detail, and solid computer literacy.Bonus Points: Project management experience and prior knowledge of ISO 9001, ISO 13485, or AS9100 are a distinct advantage (but not a dealbreaker!).Your Rewards and WellbeingWe believe in rewarding your contribution with a comprehensive package designed to support your life both inside and outside of...