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

Apply Now

Lab Technologist

Longbridge, Warwickshire
1 week ago
Create job alert

Our client, 3P innovation is a leader in the design and manufacture of automated machinery for the pharmaceutical, medical device, and FMCG industries. Based in Warwick, they are an award-winning engineering company known for our cutting-edge technology and commitment to innovation, quality, and collaboration.

If you’re looking to work on pioneering projects that make a tangible impact, and be part of a talented, multidisciplinary team, 3P innovation is the place for you.

The RoleWe are seeking a highly motivated and detail-oriented Lab Technologist to join our R&D team.
This role combines hands-on laboratory and technical work with customer interaction. You’ll plan and run pharmaceutical filling trials, prepare technical reports, support product demonstrations, and contribute to new product development and continuous improvement initiatives.

Key Responsibilities
Collaborate with the Applications Team to understand customer requirements, describe technical solutions, and demonstrate 3P’s capabilities.

Plan, set up, and run pharmaceutical filling trials (liquid and powder), ensuring compliance with safety and quality standards.

Prepare tooling, equipment, and materials for trials and demonstrations.

Analyse data and produce clear, professional technical reports.

Maintain laboratory and demonstration areas, ensuring equipment and materials are in excellent condition.

Support R&D and new product development projects with a practical, problem-solving approach.

Work closely with cross-functional teams across mechanical, electrical, and software engineering.

Develop specialist knowledge in pharmaceutical processes such as powder handling, containment, and GMP practices.

Uphold health, safety, and quality standards at all times.

About YouEssential Skills & Experience:

Hands-on experience in a laboratory, R&D, or engineering environment.

Strong technical, analytical, and problem-solving skills.

Excellent organisational and time-management abilities.

Skilled in producing clear, concise, and accurate technical reports.

Confident communicator with the ability to collaborate across teams and with clients.

Committed to maintaining high standards of safety and quality.

Proficient with MS Office (Word, Excel, PowerPoint).

Desirable:

Experience in pharmaceutical labs, manufacturing, medical devices, or other regulated industries.

Knowledge of drug product development or associated manufacturing processes.

A strong interest in science and engineering.

Qualifications
Minimum HNC/HND or degree in a science or engineering discipline.

Ideally 10 years’ experience in a relevant technical or laboratory role.

 Why Join Us?
Work on cutting-edge projects that push the boundaries of pharmaceutical and medical device technology.

Join a supportive, collaborative team that values learning and development.

Be part of a company that fosters innovation and celebrates success.

If this role sounds of interest to you, please click apply today

Related Jobs

View all jobs

Growth Partnerships Manager - Clinical Trials & Health Technology

Microfluidics Engineer – IVD / Diagnostics

Principal Human Factors Engineer - Implantable Medical Devices

Director, Regulatory Affairs Labeling

Lab Team Leader (FTC)

Lab Technician - Biomaterials

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.