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QIAGEN

Instrumentation Systems Engineer

CompanyQIAGEN
LocationManchester, England, United Kingdom
Posted At2/25/2026

UK Visa Sponsorship Analytics

Analytics are greyed out due to low classification confidence (51.0%).
Occupation Type
Production and process engineers
Occupation Code Skill LevelHigher Skilled
Sponsorship Salary Threshold
£45,000 (£23.08 per hour)
Occupation rate applies

Above analytics are generated algorithmically based on job titles and may not always be the same as the company's job classification. You can also check detailed occupation eligibility, and salary criteria on our UK Visa Eligible Occupations & Salary Thresholds page.

Disclaimer: Hunt UK Visa Sponsors aggregates job listings from publicly available sources, such as search engines, to assist with your job hunting. We do not claim affiliation with QIAGEN. For the most up-to-date job details, please visit the official website by clicking "Apply Now."

Description


Overview

At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.  

We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams. 

We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. 

At QIAGEN, every day is an opportunity to make a real-life impact. 

Join us, grow with us, and together, let's shape the future of biological discovery. 

‎

About the opportunity

We are seeking a skilled Systems Engineer to support and enhance QIAGEN’s portfolio of scientific and diagnostic instruments. In this role, you will work closely with global suppliers, manufacturing partners, and cross‑functional R&D teams to maintain, improve, and troubleshoot complex electro‑mechanical systems. You will play a key part in root cause investigations, design and DHF maintenance, change management, and system‑level improvements across our product range.

This position will suit an engineer who enjoys diving deep into complex systems, resolving systemic issues, and enabling robust, data‑driven technical decisions.

Your tasks

System Support & Improvement

  • Analyse instrument performance and identify opportunities to improve system reliability, robustness, and manufacturability.

  • Lead investigations into systemic and field‑reported issues, designing experiments to reproduce failures and determine root causes.

  • Develop, verify, and implement system or design changes in collaboration with cross‑functional engineering teams.

Design History File (DHF) & Change Management

  • Support ongoing DHF maintenance, ensuring documentation remains accurate, complete, and compliant.

  • Participate in and conduct change management activities, including impact assessments, risk evaluations, and verification planning.

Cross‑Functional Collaboration

  • Work closely with suppliers, manufacturing sites, and global R&D teams to ensure design intent, quality standards, and manufacturing processes are aligned.

  • Provide engineering expertise to teams across sample preparation, PCR workflows, troubleshooting, and system integration.

Data‑Driven Engineering

  • Plan and execute well‑designed experiments, including multifactorial studies, to inform and advise decision‑making.

  • Analyse data and present findings clearly to technical and non‑technical stakeholders.

  • Your profile

    Essential

    • Degree in Mechatronics, Mechanical, Electrical, Instrumentation Engineering, or related discipline.

    • Experience working with complex electro‑mechanical or robotic systems.

    • Strong analytical and problem‑solving skills, with hands‑on experience in root cause analysis and system‑level troubleshooting.

    • Experience working within regulated development or manufacturing environments.

    Preferred

    • 5+ years of experience in instrumentation, automation, or medical device engineering.

    • Knowledge of optical, fluidic, and mechanical subsystems.

    • Familiarity with design control processes (FDA, ISO, cGMP), CAPA, FMEA, and related quality tools.

    • Experience with PCR workflows or sample preparation technologies.

    • Proficiency with CAD tools (e.g., SolidWorks).

    • Willingness to travel internationally (up to 10%).





    What we offer  


    • Attractive pension  


    • Private Healthcare and Dentalcare  


    • Gym membership contribution  


    • A range of retail discounts and offers  


    • Enhanced maternity package  


    • Flexible working options  


    • Bonus/commission  


    • 25 days annual leave (potential to increase linked to service)  


    • Employee Assistance Program and internal QIAGEN communities  


    • Hybrid work (conditional to your role) 




    Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.   

    QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.