Be at the heart of actionFly remote-controlled drones into enemy territory to gather vital information.

Apply Now

Instrument Lifecycle Coordinator

Loughborough
1 day ago
Create job alert

Exciting Opportunity: Instrument Lifecycle Coordinator
Are you looking to take your expertise in laboratory equipment management to the next level? A leading CDMO is seeking an Instrument Lifecycle Coordinator to join their Laboratory Services team in Loughborough on a 12-month contract.

Job Title: Instrument Lifecycle Coordinator
Vacancy Type: 12-Month Contract (with potential extension)
Location: Loughborough
Salary: £14.49 per hour
Hours: 37.5 per week

About the Role

In this role, you'll be central to ensuring laboratory instruments are qualified, maintained, and compliant throughout their lifecycle. You'll work closely with internal teams and external vendors to keep projects on track and equipment operating to the highest standards. Key responsibilities include:

Coordinating qualification activities for laboratory instruments, from planning through execution and documentation
Assisting with procurement, delivery, and installation of new equipment to meet project timelines
Supporting calibration and maintenance schedules to ensure reliability and compliance
Preparing and reviewing qualification protocols, reports, and related documentation in line with GxP requirements
Acting as a point of contact for internal stakeholders and external service providers

What We're Looking For

At least 2 years' experience in a GxP-regulated pharmaceutical environment
Recent hands-on involvement in equipment qualification and calibration processes (IQ, PQ, OQ, DQ)
Familiarity with analytical instruments such as HPLC and GC
Experience using Chromatography Data Systems (e.g., Empower) and Electronic Laboratory Notebooks (ELN)
A degree in analytical sciences or a related discipline
Strong organizational skills, attention to detail, and excellent communication abilities

This is a fantastic opportunity to gain exposure to a dynamic CDMO environment and contribute to critical laboratory operations. Apply today and take the next step in your career!

For more information, please contact Selby De Klerk at SRG

SRG are the UK's number one recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.
As scientists ourselves, our specialist sector knowledge and passion are second to none. We're committed to providing outstanding career opportunities and expert recruitment services across all levels.

If this position isn't quite right for you, feel free to get in touch or visit (url removed) to explore other vacancies.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy

Related Jobs

View all jobs

Mechanical Design & Process Engineer

Head of Electronics

Vice President Regulatory Affairs

Vice President Regulatory Affairs

Vice President Regulatory Affairs

Vice President Regulatory Affairs

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Medical Technology Recruitment Trends 2025 (UK): What Job Seekers Need To Know About Today’s Hiring Process

Summary: UK medical technology hiring has shifted from title‑led CV screens to capability‑driven assessments that emphasise regulatory‑aware product delivery (QMS, ISO 13485), software lifecycle & risk (IEC 62304/14971), usability (IEC 62366), clinical & regulatory strategy (MDR/UKCA), device cyber security & privacy, and measurable patient/clinical and commercial impact. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for SaMD engineers, AI/ML in medical devices, product & quality engineers, regulatory/clinical affairs specialists, validation/verification, manufacturing/operations, and digital health roles. Who this is for: Software/firmware engineers in medtech, SaMD/AI engineers, systems & verification engineers, quality & regulatory affairs (QARA), clinical evaluation/PMCF specialists, human factors engineers, medical device cyber security & privacy, test/validation, manufacturing & operations, field/service engineers, and medtech product managers in the UK.

Why Medical Technology Careers in the UK Are Becoming More Multidisciplinary

Medical technology (medtech) is transforming healthcare in the UK — from wearable sensors to AI diagnostic tools, from surgical robots to telemedicine platforms. Advances in hardware, software, data and connectivity are enabling more personalized, efficient and accessible care. But with great power comes great responsibility. As medical devices and health technologies enter hospitals, clinics and consumers’ homes, professionals in this domain must master much more than engineering and algorithms. They must also understand law, ethics, psychology, linguistics & design. That is, medtech careers are now deeply multidisciplinary. In this article, we explore why medical technology careers in the UK are becoming more multidisciplinary, how these five allied fields now intersect with medtech work, and what job-seekers and employers should do to succeed in this evolving ecosystem.

Medical Technology Team Structures Explained: Who Does What in a Modern MedTech Department

Medical technology (MedTech) spans everything from wearable health devices and surgical robots to diagnostic imaging, in-vitro diagnostics (IVD), digital therapeutics, AI-driven triage, and Class I–III medical devices. In the UK, the sector touches NHS care pathways, private providers, and global markets—with stringent expectations for safety, clinical evidence, cybersecurity, and data privacy. As ventures scale from prototype to regulated product, clear team structures become the difference between promising pilots and licensed, market-ready devices. Whether you’re hiring your first clinical specialist or applying for a role in QA/RA, this guide explains who does what in a modern MedTech department, how functions collaborate across the product lifecycle, UK-typical skill sets and salaries, common pitfalls, and best practices for building a resilient team.