Job Opportunities API

Job Description Summary Who We Are & What We Do We are a global life sciences solutions provider, delivering agile clinical trial and diagnostic services that help our customers navigate the complexities of life‑changing innovation. With over 40 years of experience in custom kitting and clinical trial support, our Clinical Services team combines deep technical and regulatory expertise with a strong track record of delivering high‑quality products and tailored solutions that our customers trust. Based in Chorley, our Equipment & Ancillaries team provides a truly global service, sourcing and supplying medical and laboratory equipment to meet the unique needs of each study. From single-site trials to complex, multi-country programmes, we ensure our customers have the right equipment, in the right place, at the right time, enabling them to focus on delivering successful clinical outcomes, wherever their trials take place. How will you make an impact & Requirement Role Mission As a Quality Assurance Specialist, you will play a key role in   maintaining   and continuously improving the site's Quality Management System (QMS), ensuring compliance with regulatory requirements, industry standards, and customer expectations. You will support quality leadership by driving quality assurance activities, managing CAPA and audit   programmes , supporting supplier and customer quality initiatives, and leading process improvement efforts that enhance operational excellence and compliance across the business. Key Responsibilities • Support the management and continuous improvement of the site's Quality Management System (QMS), including the Quality Manual, SOPs, work instructions, forms, and associated documentation • Lead the implementation, revision, and control of quality system documentation to ensure compliance and operational effectiveness • Manage and support the CAPA   programme , ensuring   timely   investigation, implementation,   effectiveness   review, and closure of corrective and preventive actions • Plan, conduct, and lead internal audits   in accordance with   ISO 9001, ISO 13485, QSR, and other applicable standards • Support customer, supplier, and regulatory audits, including audit preparation, responses, corrective actions, and closure activities • Coordinate supplier quality activities, including supplier evaluations, performance reviews, and supplier audit   programmes • Support complaint investigations, ensuring   timely   review, escalation, resolution, and closure in line with quality requirements • Monitor quality trends and performance metrics, identifying opportunities for continuous improvement and risk reduction • Lead or support Lean, Six Sigma, Kaizen, and other continuous improvement initiatives to strengthen quality systems and operational performance • Support validation activities, including the preparation and execution of protocols, testing, and documentation where   required . • Drive the implementation and   optimisation   of quality management software systems, including ETQ Reliance modules and related tools • Deliver training and guidance on quality processes, compliance requirements, and continuous improvement methodologies. • Evaluate emerging regulations, standards, and industry best practices, providing recommendations to support ongoing compliance and business readiness • Collaborate cross- functionally   with Operations, Supply Chain, Customer Service, and Leadership teams to promote a culture of quality and continuous improvement What   We’re   Looking For We're   looking for a proactive quality professional with experience working in regulated environments and a passion for continuous improvement. You will have   strong   knowledge of quality systems, auditing, and compliance, combined with the ability to influence stakeholders and drive meaningful change. This role is ideal for someone who enjoys balancing operational quality activities with strategic improvement initiatives. Essential skills and experience: • Experience supporting or managing Quality Management Systems (QMS) within a regulated environment • Strong knowledge of quality standards and regulations, including ISO 9001, ISO 13485, FDA Quality System Regulations (21 CFR Part 820), and/or similar regulatory frameworks • Experience conducting internal audits and supporting customer, supplier, or regulatory audits • Knowledge of CAPA processes, complaint handling, non-conformance management, and root cause analysis methodologies • Strong documentation control experience, including SOP development, review, and implementation • Excellent problem-solving and analytical skills with the ability to   identify   trends and drive improvements • Experience working with quality software systems and electronic quality management systems ( eQMS ) • Strong communication   and stakeholder management skills, with the ability to   influence at   all levels of the   organisation • Excellent   organisational   skills and the ability to manage multiple priorities and deadlines • Proficiency   in Microsoft Office applications, including Word, Excel, Outlook, and PowerPoint • Ability to work independently while collaborating effectively within cross-functional teams Desirable (but not essential): • Bachelor's degree in Quality , Life Sciences, Engineering, Business, or   a related   discipline • Previous   experience within medical devices, pharmaceuticals, biotechnology, clinical trials, healthcare, or other   GxP -regulated industries • Lead Auditor qualification or formal auditing certification • Experience with ETQ Reliance or other electronic Quality Management Systems ( eQMS ) • Knowledge of EU MDR (745/2017) and IVDR (746/2017) regulations • Lean Six Sigma Green Belt certification or experience applying Lean, Six Sigma, or Kaizen methodologies • Experience supporting validation   programmes   and qualification activities • Experience managing supplier quality   programmes   and supplier audits • Project management experience, particularly within quality or compliance-focused initiatives • Experience supporting global quality or regulatory compliance   programmes What We Offer At Resonant,   we’re   more than a leading life sciences   company,we’re   a global team united by a shared purpose: the uncompromising pursuit of quality to help our customers move science forward. When you join us, you become part of a growing global community of more than 850 dedicated professionals. In return for your skills, knowledge, and experience, we are committed to helping you thrive, offering access to high-quality learning, development, and career progression opportunities so you can reach your full potential. This role is based on-site, with a requirement to work from the office for a minimum of   2 days per week   to support close collaboration and operational effectiveness. Our competitive reward package includes, following qualifying periods: • Healthcare coverage • Company bonus scheme • Pension scheme • Flexible working options • Associate engagement activities and wellbeing initiatives • Generous annual leave, plus an extra day off to celebrate your birthday Join Us Whether you bring a background in life sciences or proven operational   expertise , this is your opportunity to be part of a collaborative, high-performing team making a real difference. If   you’re   ready to take the next step in your career and help clients move their life science   programmes   forward with clarity and purpose— we’d   love to hear from you. Apply now and join Resonant.